Newsletter_05-2026_EN
A cleanroom is a room in which the concentration of airborne particles is kept very low. The lower the proportion of airborne particles in a room needs to be, the more important technology that guarantees the purity of the air becomes. Internationally, however, cleanroom technology is not an industry but an economic sector that is essential in many industries in which particles and germs are counterproductive in production, processing and handling: Pharmaceutical industry and biotechnology, chemical industry, healthcare, food industry and cosmetics, surface and plastics technology, microelectronics and microsystems technology, optics and laser technology, aerospace technology, automotive industry and electromobility as well as research and development in general. Cleanroom technology is an important regulatory and economic factor in all future-relevant industries. All of these listed industries, and probably a few more, have no future prospects in international competition without cleanrooms, because regulatory requirements define areas of use and applications: ISO-14611 series of standards and the VDI-2083 series of guidelines, the EU GMP guidelines, the ISPE Baseline Guides and the WHO Technical Report Series-No-957, as well as several more.
A cleanroom is a room in which the concentration of airborne particles is kept very low.
The lower the proportion of airborne particles in a room needs to be, the more important technology that guarantees the purity of the air becomes. Internationally, however, cleanroom technology is not an industry but an economic sector that is essential in many industries in which particles and germs are counterproductive in production, processing and handling:
Pharmaceutical industry and biotechnology, chemical industry, healthcare, food industry and cosmetics, surface and plastics technology, microelectronics and microsystems technology, optics and laser technology, aerospace technology, automotive industry and electromobility as well as research and development in general.
Cleanroom technology is an important regulatory and economic factor in all future-relevant industries.
All of these listed industries, and probably a few more, have no future prospects in international competition without cleanrooms, because regulatory requirements define areas of use and applications:
ISO-14611 series of standards and the VDI-2083 series of guidelines, the EU GMP guidelines, the ISPE Baseline Guides and the WHO Technical Report Series-No-957, as well as several more.
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EN 05/26
Molecules at
your fingertips
TITLE
toolcraft AG completes state-of-the-art cleanroom
– focus on controlling molecular contamination
Molecules at your
fingertips
The new cleanroom of toolcraft
AG is consistently designed to
control molecular contamination
(Airborne Molecular
Contamination AMC).
(Photo: CAT Group)
If it concerns contamination in a cleanroom, the primary monitoring
goal is usually „particles.“ This is not surprising, as particles are present
in the air in the millions — per cubic meter, mind you. However,
there is another form of contamination that is often underestimated
during the planning and implementation of cleanrooms: molecular
contamination (Airborne Molecular Contamination AMC). This refers
to gaseous or vaporous substances, often outgassing from materials,
process chemicals, or volatile organic compounds. Molecular
contaminations are usually much smaller than particles and can lead
to uncontrollable chemical reactions, corrosion, or film formation on
surfaces.
toolcraft AG in Georgensgmünd is now commissioning a stateof-the-art
cleanroom, whose planning and implementation were
consistently focused on controlling molecular contamination. The
specialist for additive and subtractive manufacturing technologies
as well as customized automation solutions set the highest requirements
for the environmental conditions of the approximately
600-square-meter cleanroom of ISO Class 6 from the outset.
For the implementation of this demanding project, toolcraft AG
commissioned CAT Clean Air Technology GmbH from Stuttgart.
„We were looking for a partner who not only has extensive experience
in cleanroom technology but is also absolutely proficient in the
field of molecular contamination,“ says Markus Miehling, Head of
Quality Assurance and Technical Cleaning at toolcraft.
The commissioning included, among other things, the planning
and realization of the entire ventilation, cooling, dehumidification,
and measurement and control technology, the compressed air distribution,
the cleanroom enclosure areas, and the cleanroom furniture.
Additionally, the overall coordination, commissioning, regulation,
and initial qualification.
In a remarkably short time — just under a year — the project team
completed the complex construction. About 20 toolcraft employees
will now perform component-specific assemblies for the high-tech
industry in the new cleanroom in a 3-shift operation, as well as work
in the area of cooling channel and spray cleaning.
toolcraft AG, headquartered in Middle Franconia‘s Georgensgmünd,
specializes in manufacturing high-end precision components
as well as customized automation and engineering solutions.
The family-owned company, founded in 1989, employs nearly 500
staff at two locations. Additionally, toolcraft has established a strategic
foothold in Asia through a stake in PT.YPTI in Indonesia.
CAT Clean Air Technology GmbH
Motorstraße 51
D 70499 Stuttgart
Telefon: +49 711 365919937
eMail: info@catgmbh.de
Internet: http://www.catgmbh.de
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Survey on Market
Development in
Technical Cleanliness
MAI 2026
Dear cleanroom professionals,
It’s May, and the sunshine has a positive
effect on our well-being, boosts
our energy levels and helps lift the typical
winter-economy-politics-blues.
We’ve had a look around the market and found
some interesting articles for you.
The industry of Technical Cleaning is developing more dynamically
than ever. New markets are emerging, technologies are changing
processes, and business models are noticeably shifting. Those who
do not actively evaluate these developments are increasingly making
strategic decisions in the dark.
Since 2021, the CEC has been collecting market data annually and
making developments transparent. This creates real time series and
trends that provide orientation. The current survey has been specifically
further developed and is more focused on new markets, business
models, as well as digitalization and AI.
This is exactly the added value provided by the current survey on
market development in Technical Cleaning by the Cleaning Excellence
Center (CEC).
Why participate?
The survey offers the opportunity to share your own perspective and
at the same time benefit from the results. When many companies
participate in the survey, it creates a comprehensive picture that allows
early recognition of new challenges and market requirements.
The broader the data base, the more valuable the insights for all participants.
These well-founded data can then be used for marketing,
sales, and corporate strategy.
Participants will receive the complete study afterward free of
charge, saving 120 euros.
Here’s a brief overview of the contents
of this newsletter:
> Survey on Market Development
in Technical Cleanliness
> LIFE SCIENCE READY DAYS 2026
> Cleaning pharmaceutical packaging reliably
and resource-efficiently after filling
> Cleanroom-compatible seating Systems
> When function creates atmosphere
> Synergies for high-tech cleanroom planning
> . . .
Mit freundlichem Gruß
Reinhold Schuster
Participation takes only about 10 minutes. Join now.
Here is the link to the survey: https://cec-leonberg.de/umfrage/
Deadline: 31.05.2026
CEC
D 71229 Leonberg
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Innovations, digital transformation, shaping the future together
LIFE SCIENCE READY DAYS 2026
The LIFE SCIENCE READY DAYS are the central customer conference
of the Systec & Solutions Group and will once again bring
together specialists and executives from the life science industry on
June 9 + 10, 2026, in Karlsruhe. The event offers an established platform
for exchange, inspiration, and practical solutions around modern,
future-proof production environments.
Under the motto “Innovations, Digital Transformation, Shaping
the Future Together,” the LIFE SCIENCE READY DAYS 2026 will
focus primarily on solutions for cleanroom environments in pharmaceuticals,
biotechnology, medical technology, and related regulated
sectors. Systec & Solutions will demonstrate how processes in cleanrooms
can be made efficient, safe, and compliant through innovative
technologies, automation, and digital systems.
A special highlight of the LIFE SCIENCE READY DAYS 2026 is
the keynote by Jean-Philippe Hagmann, an internationally recognized
innovation expert and thought leader. In his lecture, Hagmann
will explore how innovation culture and digital transformation can
be successfully implemented, especially in highly regulated environments
such as the life science industry. His focus is on how companies
can drive change, integrate new technologies, and achieve
sustainable future viability through collaboration.
Highlights of the LIFE SCIENCE READY DAYS 2026:
– Inspiring keynotes on innovation, digitalization, and future
trends in life science environments
– Live demonstrations of innovative hardware and software
solutions for use in cleanrooms
– Practice-oriented workshops on digitalization, standardization,
and automation of cleanroom processes
– Best practice insights from real customer projects in regulated
environments
– Networking on equal footing with industry experts
As an exclusive conference organized by Systec & Solutions, the
event is aimed at specialists and executives from cleanroom laboratories,
pharmaceutical and biotechnological production, as well as
regulated industrial environments who want to further develop their
processes and actively shape digital transformation.
Participation & Registration
Further information about the program and registration
options can be found at:
https://crm.systec-solutions.com/en-gb/life-science-readydays-2026
Jean-Philippe Hagmann
provides insights on innovation
nd digital transformation as a
eynote speaker.
Systec & Solutions GmbH
Wilhelm-Schickard-Str. 9
D 76131 Karlsruhe
Telefon: +49 721 663510
eMail: talk@systec-solutions.com
Internet: http://www.systec-solutions.com
Insights into current trends and future strategies
in the life sciences sector.
Intensive exchange and professional discussions characterize the LIFE
SCIENCE READY DAYS and create space for new perspectives.
www.reinraum.de | www.cleanroom-online.com NEWSLETTER | Ausgabe EN 05-2026
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Snow instead of ultra-pure water
To ensure that any substances which may have contaminated the outside
of vials during filling do not pose a risk to humans or the environment, the
exterior surfaces of containers are increasingly being cleaned.
(Photo credit: Bausch+Ströbel)
Cleaning pharmaceutical packaging reliably
and resource-efficiently after filling
Cleaning the exterior of pharmaceutical containers such as bottles, vials and cartridges
after filling prevents any adhering product residues from becoming a danger
to humans and the environment. This process, which is traditionally liquidbased,
consumes enormous amounts of energy and water and incurs high costs.
In order to offer a dependable but more resource-friendly solution, a leading manufacturer
of fill & finish machines participated in a joint project to investigate
the suitability of the quattroClean snow jet technology. The results confirm that
the sustainable cleaning process meets all the requirements of the pharmaceutical
industry. A basic validation carried out in parallel simplifies the approval of
the process in compliance with FDA and GMP regulations.
Taking on the challenges of the global market
and meeting them with the best technical
and most cost-effective solutions:
this is the corporate goal that has guided
Bausch+Ströbel SE + Co. KG since 1967 in
the design, manufacture, and sale of packaging
and production systems for the pharmaceutical
and related industries. What
started off with four employees has since
grown into an international group of companies
with a workforce of around 2,800 staff
and an export share of over 90%, making it
Up till now, external cleaning has generally
been a liquid-based process involving spraying
the containers with ultra-pure water and
subsequently drying them with clean compressed
air. This requires large quantities
of water to be treated in an energy-intensione
of the world’s market leaders in the field
of pharmaceutical packaging.
High-tech packaging solutions including
external cleaning after filling
High-quality pharmaceuticals in liquid and
powder form are filled into vials, bottles, syringes,
or cartridges on customer-specific
filling and finishing lines in a fully automated
process. This starts with cleaning and
sterilizing the containers and continues
through to labeling or syringe assembly.
“Due to the trend towards the use of increasingly
potent active ingredients, there
is a risk that the exterior of the containers
could be contaminated with a potentially
hazardous substance after filling. We are
therefore seeing a growing demand for solutions
to clean the outside of containers after
the filling process. Not only do ever-stricter
cleaning requirements have to be met,
but the reliable removal of product residues
must also be proved,” reports Werner Iländer,
Group Manager of Research, Technology
and Pharma Services at Bausch+Ströbel.
Dry snow jet technology instead
of ultra-pure water
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ve process and, depending on the product
being filled, to be disposed of as hazardous
waste. This not only results in high operating
costs for customers but is also a wasteful
use of drinking water, which has already
become scarce in some regions of the world.
“For these reasons, we looked around for
an alternative cleaning method that would
make this process more cost-efficient and
resource-friendly, as well as having a lower
CO2 footprint. We have been working with
the dry quattroClean snow jet cleaning
technology from acp systems for some time
and know that very high standards of cleanliness
can be achieved, depending on the
substance to be removed. However, we had
no valid data on the material compatibility
of the process,” says Werner Iländer, describing
the initial situation.
QuattroClean snow jet cleaning is a dry
process for full-surface and localized applications
that can be easily integrated into fully-automated
production lines. The cleaning
medium is liquid, recycled carbon dioxide,
which is a by-product of industrial processes
and used, among others, in the food
industry. The liquid CO2 is guided through
a wear-free two-substance ring nozzle and
expands on exiting to form fine snow crystals.
These are bundled by a separate jacket
jet of compressed air and accelerated to
supersonic speed. The easily-focused jet of
compressed air and snow develops a combination
of thermal, mechanical, solvent, and
sublimation effects on impacting on the
surface to be cleaned, which makes it highly
effective. The removed contaminants are
then extracted in the compact cleaning cell,
thus preventing re-contamination of the
product and contamination of the surroundings.
Since the crystalline carbon dioxide
sublimates completely during the process,
the cleaned residue-free surfaces are dry,
thereby eliminating the need for costly and
energy-intensive rinsing and drying steps.
With the aim of significantly reducing resource
consumption in the cleaning of medical and
pharmaceutical products, the material compatibility
and cytotoxicity of the dry quattroClean
snow jet cleaning technology was successfully
investigated in a joint project.
(Photo credit: acp Systems)
Joint project provides
the necessary evidence
Examination results with different test substances before and after cleaning.
(Image source: Bausch+Ströbel)
Microscope images of vials with existing damage show no change in the
defects before (left) and after (right) worst-case cleaning with the CO2 snow.
(Photo credit: Fraunhofer IPA)
Bausch+Ströbel therefore did not hesitate
to participate in a joint project funded by
Invest BW involving five industrial partners
as well as Fraunhofer IPA and the NMI Natural
and Medical Sciences Institute at the
University of Tübingen. In the project, the
material compatibility and cytotoxicity of
the cleaning technology was investigated
on various product surfaces typically found
in the medical and pharmaceutical sectors.
“This project was primarily about proving
that the mechanical forces of the snow
crystals do not alter, impair, or damage the
surface in any way. It was also important to
establish whether the thermal stress and/or
the chemical properties of carbon dioxide
affect the surfaces or biocompatibility of the
containers, for example by releasing cytotoxic
material components,” explained the
group manager.
In addition to glass vials, test specimens
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made of stainless steel 1.4301 and 1.4305
with different surface finishes, as well as polyetheretherketone
(PEEK), polyether (PE),
polyoxymethylene (POM), nitinol, and cobalt-chromium
were included in the studies.
To evaluate the test series, Fraunhofer
IPA examined the surfaces of the test specimens
microscopically (light and/or scanning
electron microscope) in their initial
state and after cleaning. The dry jet cleaning
process was carried out under worst-case
conditions, i.e. the middle section and edges
of the test specimens were continuously
irradiated with CO2 snow at a high pressure
of twelve bars for ten seconds. During the
subsequent microscopic examination of the
glass vials, no cracking was detected, and no
propagation of existing cracks was observed.
With the aid of a fluorescent penetrant,
it was also possible to demonstrate that the
snow crystals did not cause any additional
stress in the glass. Likewise, the abrupt exposure
to cold and the subsequent warming
of the vials to ambient temperature did not
result in the formation of any micro cracks.
Furthermore, in vitro cytotoxicity tests in
accordance with DIN EN ISO 10993-12:
2021-05 and DIN EN ISO 10993-12: 2021-
08 confirmed that the CO2 snow does not
impair cell vitality in any way. The VOC and
SVOC analyses carried out according to ISO
16017-1 yielded Tenax values within or below
the measurement limits.
GMP- and FDA-compliant process
The process therefore meets all the requirements
of the pharmaceutical industry in this
field; it is also compliant with GMP and FDA
in terms of material compatibility, meaning
that basic validation has already been achieved.
“In this project, we were able to generate
the key data for our customers and develop
a basic solution. The next step will be
to implement this in a market-ready product
that will significantly reduce operating costs
and resource consumption in external cleaning
for specific applications,” adds Werner
Iländer.
acp systems AG
Berblingerstraße 8
D 71254 Ditzingen
Telefon: +49 7156 480140
eMail: info@acp-systems.com
Internet: http://acp-systems.com
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A major milestone in propelling industry into the ångström era
Imec receives the world’s most advanced
High NA EUV system
– Imec announces the arrival of the ASML EXE:5200, the world’s most advanced
High NA EUV lithography system, in its 300mm cleanroom in Leuven.
– Operating the High NA EUV system in direct connection with state-of-the-art metrology and patterning
equipment/materials accelerates learning cycles to unlock the performance needed for sub-2nm logic
and future memory technologies, supporting the rapidly scaling AI and high-performance computing (HPC) markets.
– “With this strategic capability, imec reinforces its central role in launching the industry into the ångström era.
The tool is also set to play a pivotal role in solidifying Europe’s position as a leader in advanced
semiconductor R&D in the decades to come.” – Luc Van den hove, imec.
On March 18, 2026 imec, a world-leading
research and innovation hub in
advanced semiconductor technologies,
announced the arrival of the
ASML EXE:5200 High NA EUV lithography
system, the most advanced
lithography tool available today. With
this strategic milestone, imec reinforces
its position as the industry’s
launchpad into the ångström era, giving
its global partners ecosystem unparalleled
early access to the next generation
of chip-scaling technologies.
Integrated directly with a comprehensive
suite of patterning and metrology
tools and materials, the High NA EUV
system will empower imec and its ecosystem
partners to unlock the performance
needed to pioneer sub-2nm
logic and high-density memory technologies
that will fuel the rapid growth
of advanced AI and high-performance
computing.
Luc Van den hove, CEO of imec: “The past
two years have marked an important chapter
for High NA (0.55NA) EUV lithography,
with imec and ASML joining forces with the
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ecosystem in its joint High NA EUV Lithography Lab in Veldhoven
(The Netherlands) to pioneer High NA EUV technology. With the
installation of the EXE:5200 High NA EUV lithography system into
our 300mm cleanroom in Leuven (Belgium), we aim to bring these
High NA EUV patterning technologies to an industry-relevant
scale and to develop the next-generation High NA EUV patterning
use cases. Its unmatched resolution, improved overlay performance,
high throughput, and a new wafer stocker that improves process stability
and throughput, will give our partners a decisive advantage in
accelerating the development of sub-2nm chip technologies. As the
industry moves into the ångström era, High NA EUV will be a cornerstone
capability, and imec is proud to lead the way by offering its
partners the earliest and most comprehensive access to this technology.”
This milestone is a key element of imec’s five-year strategic partnership
with ASML supported by the EU (Chips Joint Undertaking
and IPCEI), the Flemish government, and the Dutch government.
Luc Van den hove: “As an integral part of the EU funded NanoIC pilot
line, the tool is set to play a pivotal role in strengthening Europe’s
position as a leader in advanced semiconductor R&D in the decades
to come.”
Having the ASML EXE:5200 High NA EUV lithography system in
imec’s cleanroom firmly positions imec as the most comprehensive
development environment for advanced patterning. Imec’s deep
ecosystem collaboration with leading chip manufacturers, equipment,
material and resist suppliers, mask companies, and metrology
experts will allow us to ramp up learning cycles and enhance process
stability to develop and demonstrate cutting-edge patterning for
next generation logic and memory device technology, driving breakthroughs
that will shape the future of advanced computing and AI in
the years to come.
Christophe Fouquet, CEO of ASML: “Imec’s installation of the
EXE:5200 marks an important step into the ångström era. Together,
we’re accelerating High NA EUV extendibility for the next generations
of advanced memory and compute.”
Imec anticipates the EXE:5200 High NA EUV lithography system
to be fully qualified by Q4 2026. In the meantime, the joint
ASML-imec High NA EUV lithography Lab in Veldhoven will remain
operational, ensuring continuity in the High NA EUV R&D activities
for imec and its ecosystem partners.
IMEC Belgium
BL 3001 Leuven
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EU is funding SPINS with an amount of € 50 million
Semiconductor-based
Quantum Pilot Line ‘SPINS’
launched with EU support
In April, ‘SPINS’ (Semiconductor Pilot line for Industrial Quantum NanoSystems)
was launched, one of the 6 European quantum pilot lines. Coordinated by
imec, the consortium brings together 25 European RTOs, industry partners, and
academic research groups to strengthen Europe’s leadership and sovereignty in
this strategically important domain. The €50 million SPINS pilot line project has
been made possible through the co‐funding support from the European Union’s
Chips Joint Undertaking (Chips JU) and the national and regional authorities of
the participating Member States. Fraunhofer IPMS plays a central role within
SPINS in the high-resolution structuring of qubit and processor elements.
tion navigation systems.
However, a gap remains between current
quantum research and manufacturable
quantum processors to enable significant
quantum applications. Scaling the number
of stable qubits (to as much as one billion)
Fraunhofer IPMS plays a central role within SPINS in the high-resolution structuring
of qubit and processor elements. © Fraunhofer IPMS
Quantum computing has become a highly
strategic domain with economic and societal
relevance rising sharply. Applications
vary from breakthroughs in drug
discovery and materials science to ultrasecure
communications and next-generais
key to building reliable and fault-tolerant
quantum computers.
Given the technological complexity, including
cryogenic operation, ultraprecise
control electronics and highly specialized
fabrication processes, and given the strategic
importance of quantum chips, the EU
Chips Act has established six complementary
quantum pilot lines, each focused on a
distinct hardware platform and collectively
advancing quantum technologies in the
space of quantum computing, communications
and sensing. Within this portfolio,
SPINS is the pilot line dedicated to semiconductor‐based
spin qubits, with a primary
focus on delivering quantum chips for quantum‐computing
applications.
Imec coordinates this new pilot line efforts
and leads the European consortium of
25 partners, ranging from RTOs like Fraunhofer,
VTT and CEA-Leti, industry (both
large enterprises like Infineon and Siltronic
as well as SMEs and startups) and academic
groups (like TU Delft and University of Jyväskylä),
bringing in complementary knowledge
and skills, with the goal of translating
the strategic framework of the EU Chips Act
into concrete actions.
The first actions of the SPINS-consortium
include process and design optimization
to establish a robust foundation for scalable,
stable, and high-performing spin qubits,
all on three different technology platforms:
Si/SiGe, Ge/GeSi, and SOI. SPINS aims to
establish a lab-to-fab route for this technology
via Multi-Project Wafers (MPW) and
standardized quantum Process Design Kits
(PDKs), which lower entry barriers for startups
and SMEs in semiconducting quantum
technology and lay the foundations for European
companies to build quantum knowhow
early on.
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Fraunhofer IPMS within the SPINS pilot line
Fraunhofer IPMS plays a central role within SPINS in the high-resolution
structuring of qubit and processor elements. All lithography
steps requiring resolutions beyond the capabilities of optical
methods are performed at Fraunhofer IPMS. This enables precise,
reproducible patterning, which is essential for the functionality and
scalability of Si/SiGe-based quantum chips. In addition, Fraunhofer
IPMS makes key contributions to process stability and maturity
across the pilot line by providing state-of-the-art cleanroom infrastructure
designed for reproducible, scalable qubit fabrication. Processes
at Fraunhofer IPMS are designed to support both Si/SiGe and
Ge/SiGe platforms, securing multiple technologically complementary
pathways within the SPINS consortium. Furthermore, the expertise
of Fraunhofer IPMS bridges to activities within the EU project
QLSI2, where migration to high-resolution lithography and 300-mm
wafers is being explored. This prepares the transfer of SPINS pilot
line results to a future 300-mm CMOS line at an early stage.
In this way, Fraunhofer IPMS combines leading research expertise
with industrial process readiness, significantly strengthening Europe’s
technological independence in semiconductor quantum technology.
European quantum pilot lines
Complementary tracks of the European quantum efforts, next to
the semiconductor-based pilot line, include pilot lines on photonics
for quantum ‘P4Q’ (coordinated by University of Twente,
NL) - to which imec is also contributing, ion trap qubits ‘CHAMP-
ION’ (coordinated by SAL, AT), superconducting qubits ‘SUP-
REME’ (coordinated by VTT, FI), diamond quantum chips ‘DI-
REQT’ (coordinated by CNR, IT) and neutral atoms ‘Q PLANET’
(coordinated by Pasqal, FR).
Fraunhofer-Institut für Photonische Mikrosysteme IPMS
D 01109 Dresden
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Uni Siegen
becomes a beacon
for intelligent
sensor technology
The University of Siegen is significantly expanding its infrastructure
for modern sensor technologies: With the WI-
SENT pilot line, a state-of-the-art environment for the development
of intelligent sensors is being created in the new
INCYTE research building. The project has a total volume of
4.7 million euros.
© Sascha Hüttenhain
Glaringly bright light, absolutely clean air, researchers in blue fullbody
suits: The cleanroom area forms the technological heart of the
new INCYTE research building at the University of Siegen. A stateof-the-art
laboratory environment in which intelligent sensors can
be manufactured, tested and developed into prototypes. The WI-
SENT pilot line is now significantly expanding the infrastructure
once again: five new high-tech systems and additional process options
are taking research and development work in the clean room to
a new level. The project is being funded by the ERDF program with
EU funds amounting to 4.7 million euros.
Partner for the industry
„The new systems not only complement the existing infrastructure,
they also enable fundamentally new process and analysis methods
and, together, create truly outstanding technological conditions. A
few years ago, we would never have dared to dream of coating or removing
individual atomic layers of selected materials in a targeted
manner,“ says Dr. Andreas Bablich, Head of Technology at WISENT.
WISENT stands for „Westphalian Intelligent Sensor Integration Pilot
Line“ - an end-to-end high-tech production line that covers the
entire development process: from the initial idea to chip and component
design, sensor production, integration into complex systems
and system-specific software development. Not only researchers,
but also companies and start-ups can make use of the infrastructure
and scientific expertise at INCYTE.
„Collaboration with industry is very important to us. We want to
create a low-threshold offer to implement feasibility studies and initial
demonstrators for new sensor concepts without companies having
to invest in cost-intensive large-scale equipment themselves,“
explain Paul Kienitz, who is responsible for operating the new cleanroom
facilities at WISENT, and Maurice Müller, who played a key
role in acquiring the pilot line.
Sensors for medicine, industry and the environment
The new infrastructure opens up a wide range of possibilities for
intelligent sensor technology: one example is 3D image sensors, in
Working together on the WISENT project: Matthias Weber,
Dr. Andrii Nehrych, PD Dr. Andreas Bablich, Prof. Dr. Peter Haring Bolívar,
Prof. Dr. Benjamin Butz, Prof. Dr. Ivo Ihrke, Prof. Dr. Michael Möller,
Prof. Dr. Bhaskar Choubey, Paul Kienitz, Moin Diwan (from left to right).
© Dirk Manderbach
The cleanroom at INCYTE may only be entered with special protective
clothing. First row: Prof. Dr. Bhaskar Choubey, Paul Kienitz,
PD Dr. Andreas Bablich, Moin Diwan, second row: Prof. Dr. Michael Möller,
Matthias Weber, Prof. Dr. Peter Haring Bolívar,
third row: Prof. Dr. Benjamin Butz, Prof. Dr. Ivo Ihrke, Dr. Andrii Nehrych
(from left to right). © Dirk Manderbach
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© Dirk Manderbach
which microscopically small structures - such as lenses or
other optical elements - can be printed directly onto the
sensor chips using modern production technologies. This
allows the incident light to be captured and processed particularly
efficiently. Novel materials also play an important
role. For example, researchers are working with extremely
thin semiconductor layers or two-dimensional materials
such as graphene.
„The integration of special AI hardware makes these
high-performance sensors even more powerful,“ explains
Dr. Bablich. „You get a kind of integrated little brain that evaluates
the huge amounts of data from the 3D pixels or graphene
layers directly on site in fractions of a second.“ This
results in extremely compact systems that perceive the environment
in precise 3D depth and immediately interpret
the information obtained. Areas of application include autonomous
driving, robotics and wearables for fall detection,
which can react in real time.
Plant analysis and biomarker recognition
Other applications range from agriculture to medicine. In
future, drones equipped with special image sensors could
analyze plants from the air and determine the health status
of fields based on reflected light signals. In medical technology,
Prof. Dr. Peter Haring Bolívar‘s team is working on
highly sensitive sensors that can detect the smallest molecules
- so-called biomarkers. This could enable diseases
such as skin cancer to be diagnosed much more effectively
in future than with current laboratory methods.
With the Center for Sensor Systems (ZESS), the University
of Siegen has already had an internationally recognized
platform for research into this key area of technology for
many years. The WISENT pilot line in the new INCYTE research
building will enable the university to further expand
its role as an innovation driver for intelligent sensor systems.
„The combination of state-of-the-art infrastructure, interdisciplinary
research and close cooperation with industry
characterizes our location. This makes us the central point
of contact in NRW for all questions relating to software,
hardware and system integration in sensor technology,“ says
Andreas Bablich.
Universität Siegen
D 57076 Siegen
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Wafer Exchange For Ferroelectric Memory
Materials Within the FAMES Pilot Line
CEA-Leti and Fraunhofer IPMS have successfully completed the first exchange
of ferroelectric memory wafers within the FAMES Pilot Line, marking a pivotal
milestone in establishing a shared European platform for advanced embedded
non-volatile memory technologies. Launched in December 2023 and coordinated
by CEA-Leti, the five-year initiative has demonstrated the viability of circulating
complex material stacks across some of its leading research fabs.
The collaboration has been first focused on
the processing and electrical characterization
of hafnium-zirconium oxide (HZO)
ferroelectric capacitor stacks. Utilizing the
combined 300 mm CMOS cleanroom capabilities
of both institutes, the wafers were
circulated in short process loops to enable
joint evaluation of materials, electrode configurations,
and device behavior.
The work also validated the wafer exchange
and contamination-control protocols
implemented in the Pilot Line, demonstrating
that complex material stacks can be
processed reliably across multiple advanced
semiconductor facilities, on all wafers.
The entire process adhered to standardized
contamination control procedures, verified
through VPD-ICP-MS (Vapor Phase
Decomposition – Inductively Coupled Plasma
Mass Spectrometry) and TXRF (Total
Reflection X-Ray Fluorescence) analytics.
Devices were evaluated using a FeCAP array
test vehicle designed by CEA-Leti, with
electrical characterization performed via
the PUND (Positive-Up-Negative-Down)
methodology to isolate true ferroelectric
switching from parasitic effects.
Accelerating the Path Toward
System-Level Application
„The successful wafer exchange marks an
important step toward a joint European
material testing platform for ferroelectric
memories,“ said Dr. Wenke Weinreich, Division
Director of Fraunhofer IPMS’ Center
Nanoelectronic Technologies, a member of
the 11-member consortium. „By combining
our processing expertise with CEA-Leti’s
CMOS integration capabilities, the pilot
line provides a powerful environment for
evaluating new ferroelectric stacks and accelerating
their path toward system-level
applications.“
Initial experimental results have already
yielded critical insights. The team screened
various electrode materials to enhance
performance, finding that titanium nitride
Illustration of HfO₂-based ferroelectric devices enabling scalable, CMOS-compatible non-volatile
memory. The architecture supports integration in both front-end (FeFET) and back-end memory
structures, while opening pathways to advanced ferroelectric functionalities such as multiferroic,
pyroelectric, and tunable RF devices. © Fraunhofer IPMS
(TiN) bottom electrodes significantly outperform
tungsten (W). In reliability tests,
TiN exhibited lower failure rates after 10⁷
field cycles at 4 MV/cm. Furthermore, clear
cross-split effects were observed across different
electrode configurations, confirming
the sensitivity of the test vehicles to process
variations.
Seamless Exchanges Across FAMES’ Sites
„This first exchange between CEA-Leti and
Fraunhofer IPMS demonstrates that shared
process flows, test vehicles, and characterization
environments can work seamlessly
across FAMES’ sites,“ noted project Coordinator
Dominique Noguet. „Establishing reliable
wafer loops between leading research
fabs is essential for accelerating ferroelectric
memory development.“
Looking ahead, the wafer loops lay the
groundwork for broader collaborative development.
Upcoming phases will integrate
HfO₂-based ferroelectric stacks from
Fraunhofer IPMS into CEA-Leti CMOS
processes, followed by array-level evaluations
of state-of-the-art memory technologies
embedded in the upcoming Global-
Foundries’ 22nm FDX® Memory Advanced
Demonstrator Multi Project Wafers shuttle
prepared by CEA-Leti. The roadmap also
includes studies on electrode process variations,
long-term reliability, and back-endof-line
integration approaches.
In parallel, Fraunhofer IPMS recently
completed a first chip tape-out using GlobalFoundries’
22nm FDX® technology and
initiated research on algorithm-based AI
compute-in-memory accelerator architectures
built on these ferroelectric technologies.
Together, these efforts advance the core
mission of the FAMES Pilot Line: to provide
a unified European platform for developing
and validating emerging memory technologies—including
OxRAM, MRAM, FeRAM,
and FeFET. By enabling collaborative material
development and standardized characterization,
the initiative aims to strengthen
Europe’s capacity to design and manufacture
the low-power, next-generation chip architectures
required for the future of computing.
Fraunhofer-Institut für
Photonische Mikrosysteme IPMS
D 01109 Dresden
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Highest hygiene: Stainless steel,
rust-free, for tray handling systems
Granulation systems with stainless steel components
ensure efficient granulation. © L.B. Bohle
Tablets are among the most widespread forms of medication,
nutraceuticals, and dietary supplements. Easy to dose,
convenient to transport, and to take with a sip of water whenever
needed, they ensure precise release of active ingredients.
Their production demands the highest standards:
consistently high quality and compliance with all regulations
for process and food safety must be balanced with resource-efficient,
sustainable manufacturing and cost-effectiveness.
Tablet presses, which can be flexibly used for
batch and high-volume production, automate and control
the complex process from powder to finished tablet. The
heart of these production lines are tablet presses, as they
significantly contribute to the quality, safety, and economic
efficiency of the products. For all parts in contact with the
product, high-quality stainless steel, corrosion-resistant, is
mandatory.
Diverse types of tablets – single or multilayer, coat-core, effervescent,
or lozenges – as well as various tablet shapes require tailored
equipment concepts. The range of tablet presses extends from laboratory
eccentric presses for initial feasibility studies, through R&D
rotary presses, standard single and multi-station rotary presses, to
high-performance double rotary presses. Fully integrated systems in
enclosed design with containment features for highly active or toxic
substances encompass the entire production process, from material
feeding, dosing, granulation, to tableting and quality control, packaging
into blisters or cans, as well as cleaning, retooling, and maintenance
of all system components.
Fundamental components of every tablet press include hoppers,
feed shoes, dies, and punches. Besides the active pharmaceutical
ingredient, tablets usually contain additional excipients such as binders,
lubricants, and flow regulators. A balanced interplay of these
components is crucial for the flow properties of the material. Granulates
have better flow characteristics compared to powders and
can therefore be dosed more effectively. Various processes such as
fluidized bed, vertical, high-shear, or double-screw granulation are
used industrially to produce granulates for tablets. Batch granulators
combine three process steps in one vessel: mixing, vertical or highshear
wet granulation, and drying.
Up to one million tablets per hour
The use of stainless steel in tablet manufacturing equipment significantly
contributes to the quality, safety, and cost-effectiveness of the products.
© L.B. Bohle
The powder or granulate mixture is fed into the hopper, which distributes
it into openings called dies, determining the later tablet shape,
on a rotating die wheel. Die segments can replace the rotor to enable
significantly more tablet stations at the same press size. In the dies,
upper and lower punches compress the material with increasing
force into the final tablet shape. Often, tablets are also marked with
a break line and a logo here.
Sensors measure the pressing force and ensure consistent quality
by monitoring weight, hardness, thickness, and breaking strength
of each individual tablet. Some press models address the high load
on tooling with heavy-duty profile heads to minimize wear. The
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In integrated plant concepts for tablet manufacturing, product-contact
components made of stainless steel corrosion-resistant provide the
necessary product safety across processes. © L.B. Bohle
For equipment enclosures,
stainless steel is the guarantee
of sustainably highest hygiene
and reliable durability in 24/7
operation. © FETTE Compacting
When it comes to stainless steel
tablet presses, product quality and
process safety are the focus.
© FETTE Compacting
finished tablet is pushed upward from the die by the lower punch
and transported into a collection container or onto a conveyor belt
by a shuttle. High-performance presses process all types of granulate
and viscous products at high speed using changeable die discs. They
can produce over a million single-layer tablets in various shapes or
up to 500,000 multilayer tablets per hour.
Protection against emissions through containment features
Stainless steel, due to its corrosion resistance and good processing
properties, is a standard material for numerous components in
tablet manufacturing equipment. © WZV/ERWEKA
High-quality stainless steel, rust-free, meets the strictest
hygienic requirements through its smooth, abrasion-resistant,
and easy-to-clean surface. © L.B. Bohle
Ensuring process safety also involves protecting people and the environment
from emissions. Product changeovers require the press
to be thoroughly cleaned beforehand to prevent cross-contamination.
Increasing demands for active ingredient safety and process
control are reflected in various containment features in tablet production.
Modern tablet presses are designed with dust-tight basic
equipment and operate under vacuum to prevent active ingredient
escape. When processing highly active or toxic substances, a fully
enclosed system with complete containment features is necessary.
The five-stage containment pyramid from the International Society
for Pharmaceutical Engineering (ISPE), known as the Occupational
Exposure Band (OEB), is used to classify the hazard level of the substances
used.
In practice, for products rated OEB 3 and above, fully automated
tablet production from system filling to dust-minimized tablet
discharge is considered the minimum standard. Glove boxes, leakproof
transfer systems, and efficient dry and wet cleaning technologies
complement containment solutions. From OEB 4 onwards,
Wash-in-Place (WIP) procedures significantly reduce the workload
for machine operators during cleaning. For hazard class OEB 5, the
highest safety requirements in production and personnel protection
are ensured by a highly complex high-containment system for
the entire plant: including a closed material handling system with
fully enclosed, integrated production lines from automatic material
feeding, tableting, in-process quality control, comprehensive dust
emission control, air management, and Wash-in-Place technology.
For highly active active pharmaceutical ingredients, whose demand
is rapidly increasing due to new therapies, such as in oncology,
continuous direct compression in a closed system is considered a
future-oriented solution.
Cross-process use of stainless steel
In tablet manufacturing systems, components made of stainless
steel – like this measuring machine – provide reliable protection against
emissions and cross-contamination. © FETTE Compacting
Given strict requirements for hygiene and purity of the production
environment according to ISO standards or Good Manufacturing
Practice (GMP), stainless steel is indispensable for all product-con-
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The use of stainless steel (stainless) in this fully automatic
tablet hardness tester guarantees a hygienic production
environment. © WZV/ERWEKA
tact components in tablet production lines. High-quality stainless
steel, such as grades 1.4404 and 1.4435, meets the strictest hygienic
standards due to its smooth, wear-resistant, and easy-to-clean surface.
The durable surface quality of this inert material withstands
corrosive environments, high pressures, and temperatures over the
long term. Particularly, austenitic stainless steel 1.4404 with 2 to 2.5
percent molybdenum content is a standard material for many components
in integrated production lines due to its corrosion resistance
and good processing properties.
Electropolished surfaces with defined roughness prevent particle
adhesion, further increase corrosion resistance, and withstand
mechanical stresses. Appropriately designed stainless steel components
in tablet systems are fully WIP-compatible and can be cleaned
repeatedly without residue. In integrated tablet manufacturing
systems, product-contact components made of corrosion-resistant
stainless steel provide the necessary process safety and reliable protection
against emissions and cross-contamination across the entire
process chain.
From IBC containers for raw material and product storage, to
granulators, mixers, hoppers, dies, and punches, up to conveyor
belts, sampling systems, waste disposal units with metal detectors,
sorting and counting systems, high-quality stainless steel is standard
practice. It is also used in dust extraction filters, air filters, cleaning
systems, sensor and control housings, and plant enclosures, ensuring
maximum hygiene and reliable durability in 24/7 operation.
Warenzeichenverband Edelstahl Rostfrei e.V.
D 40237 Düsseldorf
Alles für Ihren Reinraum
aus einer Hand
Bekleidung & Handschuhe
Tücher & Swaps
Reinigungsgeräte- & mittel
Dispenser
Partikelmessgeräte
Staubbindematten
HANS J. MICHAEL GmbH, Hart 11, 71554 Weissach im Tal
hjm-reinraum.de | Tel. 07191/9105-0 | office@hjm-reinraum.de
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Why the right office chair contributes more to process safety than often assumed
Cleanroom-compatible seating systems
In cleanrooms, every detail is crucial. Air purity, material behavior,
cleanability, and electrostatic safety must be precisely coordinated
to ensure stable processes and consistent product quality. While
machines, materials, and process media are usually thoroughly evaluated
and monitored, one element is often underestimated in daily
practice: the work chair.
However, a cleanroom chair is much more than just a seat. It is
located in close proximity to the process, interacts directly with the
operating personnel, and influences both hygiene and ergonomics
as well as process stability. Those who think holistically about cleanroom
workstations should therefore consider seating systems under
the same criteria as other technical components.
Cleanroom workstations impose special requirements
Depending on the industry — such as semiconductor manufacturing,
medical technology, pharmaceuticals, or precision mechanics — uncompromising
requirements apply in the cleanroom. Components
used in these environments must behave controllably, be safely cleanable,
and must not introduce additional contamination sources.
For seating systems, this means specifically: they must not only
be ergonomic but also designed structurally and materially for cleanroom
use. Particularly in sensitive areas according to DIN EN ISO
14644-1, aspects such as particle emission, cleanability, material stability,
and ESD safety play a central role.
Hygienic Design: Cleanability begins in the construction
A cleanroom-compatible work chair must be designed so that surfaces
can be cleaned quickly, thoroughly, and safely. This is precisely
where the principle of Hygienic Design comes into play.
For Bimos, this means for a cleanroom chair like the TEXON:
– Smooth, closed surfaces
– Minimized joints and gaps
– Rounded transitions
– Sealed mechanisms
– Easily accessible cleaning areas
Especially in the cleanroom, open mechanisms, hard-to-reach interspaces,
or unsuitable surfaces can lead to the accumulation of particles,
residues, or lubricants. A design with a clean, reduced form
language is therefore not only a matter of aesthetics but also a crucial
contribution to process safety.
The TEXON demonstrates this approach particularly clearly:
The Clean Cover additionally protects the mechanism, the closed
design supports cleanability, and reduces potential weak points during
daily use.
Material durability is not a detail but a necessity
In addition to construction, material choice also plays a central role.
In cleanrooms, work chairs are regularly cleaned with alcohol-based
or oxidative disinfectants. Materials must therefore remain permanently
resilient — without swelling, dispersing, or altering their surface.
With Skintec, Bimos has developed a covering material specifically
designed for these requirements. The material is disinfectantresistant,
easy to clean, has a closed surface, and at the same time
offers particularly comfortable seating.
This combination is especially critical in practice: In the cleanroom,
it is not enough for a material to be merely hygienic. It must
also withstand continuous use — under mechanical stress, during
regular disinfection, and over long usage cycles.
Skintec was therefore developed to be not only functional but
also durable and economical. The surface remains dimensionally
stable, resistant to common disinfectants, and offers a high-quality
tactile feel. For companies, this means less material fatigue, longer
service life, and an overall more stable workplace standard.
Particle control also begins with sitting
Operating personnel are among the largest sources of particles in
the cleanroom. That is why the work chair influences particle control
more than often assumed.
Seating systems affect, among other factors:
– Movement patterns at the workstation
– Wear on contact surfaces
– Stability of working positions
– Material behavior during daily use
An ergonomically unfavorable chair often leads to frequent position
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Therefore, modular seating systems are increasingly important. For
example, on the TEXON, seat and backrest cushions can be quickly
and easily replaced as exchangeable pads. This not only reduces
downtime but also facilitates cleaning, maintenance, and long-term
use.
This is a real advantage especially in sensitive production environments:
individual components can be replaced without having
to replace the entire seating system. This saves resources, reduces
costs, and supports a more sustainable workplace design.
Ergonomics is also a cleanroom issue
Ergonomics is still often reduced in the cleanroom to “seating comfort.”
In reality, it is a key factor for concentration, process safety, and
work quality.
Anyone working in controlled environments for extended
periods needs a seating solution that:
– Supports an upright, stable posture
– Distributes pressure evenly
– Allows movement without creating instability
– Can be used intuitively and without distraction
changes, unnecessary compensatory movements, and potentially
increased particle disturbance. Therefore, cleanroom-compatible
seating solutions should be designed not only with low emissions
but also with ergonomic considerations.
The TEXON was developed precisely from this perspective. Its
movement mechanism supports dynamic sitting and promotes a
stable, ergonomically sensible working posture — without complicated
adjustment logic. This helps employees focus on their tasks and
reduces unnecessary movement impulses in the sensitive work environment.
ESD safety is indispensable even in the cleanroom
In many cleanroom applications — especially in electronics and semiconductor
manufacturing — not only cleanliness but also electrostatic
safety is critical. Uncontrolled discharges can damage sensitive
components or disrupt processes.
Therefore, cleanroom chairs must often be designed to be not
only particle-safe but also electrostatically safe. Bimos consistently
considers these requirements: In the TEXON, all relevant components
are conductive and tailored for use in sensitive high-tech environments.
Particularly noteworthy is a technological advancement long
considered challenging in the industry: conductive materials in light
color variants. While ESD-capable plastics have so far mostly been
realized only in dark shades, this development opens new possibilities
for light, hygienic-looking cleanroom workstations — without
compromising functionality.
Modularity and maintenance: An often underestimated advantage
Another important aspect in the cleanroom is how components
can be maintained, replaced, and used long-term. Any unnecessary
maintenance or complete replacement can interrupt processes and
incur additional costs.
This shows clearly that cleanroom chairs must not only be “cleanroom-compatible”
but also workplace-appropriate. Only when hygiene,
technology, and ergonomics are considered together does a
workplace truly meet the requirements of modern cleanroom production.
Thinking about cleanroom workstations holistically
A work chair is not a secondary element in the cleanroom. It is part
of a sensitive overall system and should be evaluated accordingly.
Construction, material, cleanability, ESD capability, ergonomics, and
maintenance all influence how stable and safe a workstation functions
in everyday use.
With solutions like the TEXON and the specially developed covering
material Skintec, Bimos demonstrates how modern cleanroom
seating systems can meet these requirements: through consistent
Hygienic Design, tested material durability, high ergonomic
quality, and technical design for sensitive production environments.
Conclusion
Cleanroom-compatible seating systems provide much more than
ergonomic support. They contribute to cleanability, particle control,
ESD safety, and long-term process stability — and should therefore
be understood as a functional component of the entire cleanroom
concept.
Those who want to future-proof cleanroom workstations should
not see the work chair as a marginal component but as a core part of
a holistically planned, standards-oriented workstation system.
Bimos - eine Marke der Interstuhl Büromöbel GmbH & Co. KG
Brühlstraße 21
Telefon: +49 7436 8710
Telefax: +49 7436 871110
eMail: bimos@bimos.com
D 72469 Meßstetten-Tieringen
Internet: http://www.bimos.com
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Moqlero - Automated Trending according to GMP Annex 1
Trends at the push of a button?
Why now is the right time to rethink
Trending in GMP Annex 1 – From „Nice-to-have“
to Regulatory Requirement
With the revision of EU GMP Annex 1 in 2022, the regulatory environment
for the manufacturing of sterile medicines has fundamentally
changed. A central element of this revision is the mandatory
introduction of systematic trending of monitoring data.
What was once considered a supportive quality tool is now an
integral part of compliance – and thus comes into focus for quality
assurance, production, and inspections alike.
From Reacting to Proactive Thinking
Trending describes the systematic, temporal analysis of monitoring
data to identify patterns, changes, and potential risks early on. Unlike
isolated consideration of individual limit breaches, developments
over longer periods become visible. The regulatory requirement is
clear: companies should no longer just react to deviations, but proactively
identify and prevent process deteriorations.
Annex 1 makes Trending Mandatory
In the revised Annex 1, especially in Chapter 9 („Environmental and
Process Monitoring“), trending is explicitly required and thus becomes
a mandatory component of environmental monitoring and the
Contamination Control Strategy (CCS).
A systematic evaluation of monitoring data is required to detect
trends, insidious changes, and recurring patterns early and to incorporate
them into the quality strategy.
This makes it clear: trending is no longer an optional reporting
tool, but a central control instrument to ensure product quality and
patient safety.
Requirements for Effective Trending
The Annex 1 sets clear expectations for implementation:
– Detection of trend patterns
Increasing limit breaches, recurring deviations, or consecutive
warning messages must be systematically recognized and
evaluated.
– Short- and long-term analysis
Both short-term events and long-term developments
are to be analyzed.
– Correlation with root cause analysis
Trending must be correlated with influencing factors such as
maintenance, personnel movements, or process changes and
forms the basis for root cause analysis and CAPA processes.
– Visualization and data preparation
Only through appropriate representations such as diagrams,
dashboards, and statistical evaluations do trends become
understandable and assessable.
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When Excel Reaches Its Limits
In practice, a clear tension emerges between regulatory demands
and real-world application, as monitoring data are still often exported,
consolidated in Excel, and manually evaluated – an approach
that increasingly reaches its limits under today‘s requirements due
to high time consumption, lack of standardization, increased susceptibility
to errors, and limited traceability.
Automation as a Logical Consequence
Automated systems address exactly this point: they enable continuous
processing of data – from collection to analysis to structured
presentation of results. Trends can be analyzed regularly, patterns recognized
early, and evaluations standardized. Results are automatically
presented both graphically and in tables, making developments
immediately traceable.
Trending at the push of a button is less about simplifying and
more about a well-defined process. After setting the parameters,
evaluations can be retrieved in Moqlero with minimal effort. For
many in practice, this means a clear break from time-consuming,
error-prone Excel processes: instead of spending hours on manual
data preparation, reliable results are available in seconds – standardized,
audit-proof, and accessible at any time.
A Look into Practice
What sounds complex in theory has long become reality in practice.
Moqlero demonstrates impressively what Industry 4.0 cleanroom
monitoring can look like.
Whether particle concentration, filter test, or air exchange rate
– the platform initially automates mobile measurements of all kinds.
And this opens up new possibilities: since all measurement results
are available digitally natively, the new GMP Annex 1 trending requirements
can be seamlessly fulfilled. Trend reports with graphics,
tables, comments, and electronic signatures are generated without
media discontinuities, with just a few clicks.
Moqlero offers six different types of trends:
– Filter efficiency, for evaluating long-term filtration performance
– Filter differential pressure, for early detection of clogging trends
– Particle counts, for identifying contamination developments
– Physical environmental parameters such as temperature and
humidity
– Air volume flow, to ensure stable ventilation conditions
– Air change rate, for further verification of cleanroom compliance
Between Obligation and Opportunity
The requirements of Annex 1 may seem demanding at first glance
– but they offer the chance to fundamentally improve quality processes.
Consistent trending increases process stability, improves data
quality, and reduces deviations and risks in the long term. Those still
relying on manual processes risk not only compliance gaps but also
valuable time that could be spent on what truly matters: quality and
patient safety.
Getting started doesn‘t have to be difficult:
With Moqlero, automated trending can be set up quickly and is
ready for immediate use – new insights, no upfront investments, and
full compliance.
Conclusion
With the new EU GMP Annex 1, trending is finally moving from an
optional tool to a regulatory obligation. At the same time, this development
marks a fundamental change in the quality understanding
of the pharmaceutical industry. The future no longer lies in retrospective
data analysis, but in its digital, intelligent utilization.
Automated trending with Moqlero exemplifies a modern, integrated
quality approach that meets the increasing demands for transparency,
data integrity, and patient safety.
For pharmaceutical companies, the question is no longer whether
this approach will be implemented, but how quickly a sustainable
and future-proof implementation can be achieved.
MKL Ingenieurgesellschaft mbH
D 81827 München
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GEA opens new technology center,
strengthening its position in the
growing pharma applications market
Together with Mona Neubaur, Minister of Economic Affairs
of the German state of North Rhine-Westphalia, GEA CEO
Stefan Klebert has opened a new technology center for pharmaceutical
freeze-drying systems in Elsdorf, Germany. GEA
employs approximately 260 people at the facility, which
combines research and development with production and
service under one roof. The site is carbon-neutral thanks to
power supplied by photovoltaic systems. The investment of
more than EUR 80 million underscores GEA’s commitment
to strengthening its position as a technology partner for the
growing global pharmaceutical industry. At the same time,
the company is making a positive contribution to structural
change in Germany’s Rhineland lignite mining region.
At the opening ceremony, GEA CEO Stefan Klebert said: “With our
new technology center in Elsdorf, we are investing in one of our key
growth areas and further strengthening our innovative capabilities
in the pharmaceutical sector. We are also significantly expanding
our production capacities. Together, these measures help us expand
our leading position in this highly innovative market segment.”
Mona Neubaur, Deputy Minister President and Minister of Economic
Affairs of the German state of North Rhine-Westphalia, was
a guest at the opening. “Today is a good day for the future of Elsdorf
and the entire region. From the heart of North Rhine-Westphalia,
GEA Group is driving the global transformation towards climateneutral
production. Efficient, digitally networked production methods
and sustainable technologies are helping to drive the transition
toward a resilient and climate-neutral economy. Elsdorf demonstrates
that North Rhine-Westphalia offers reliable framework conditions
to enable investments with significant impact. This way, we secure
good jobs, industrial value creation, and competitiveness, even
in challenging times.”
Digital on the inside, green on the outside
GEA opened a new pharmaceutical technology center
in Elsdorf (North Rhine-Westphalia). (Photo: GEA)
The new building in Elsdorf replaces an existing GEA freeze-drying
plant in neighboring Hürth, where production capacities had
reached their limits. The more than 260 employees will find ideal
conditions for their work in development, design, manufacturing,
assembly, and service at the new location. Production capacities can
be expanded, particularly through shorter production times.
Photovoltaic systems and green roofs on the production facilities
and office buildings will ensure carbon-neutral operation. GEA
uses the electricity from the roof to operate air-to-water heat pumps
for freeze-drying, heating and cooling at the site. This can save up
to 7,000 metric tons of CO₂ annually in production. Moreover, the
photovoltaic system powers 30 charging stations for e-cars and fleet
vehicles as well as six stations for e-bikes. As much of the approximately
45,000 square meter site as possible remained unsealed
thanks to the use of grass pavers.
A leader in pharmaceutical freeze-drying
Opening of the new GEA Pharma Technology Center in Elsdorf:
Johannes Giloth (COO, GEA), Michael Asenkerschbaumer (Managing
Director Lyophilization), Andreas Heller (Mayor of Elsdorf), Prof. Dieter
Kempf (Chairman of the Supervisory Board, GEA), Mona Neubaur
(Minister of Economic Affairs of North Rhine-Westphalia) and GEA
CEO Stefan Klebert (front row, from left to right). (Photo: GEA)
Freeze-drying is a necessary production step for many temperaturesensitive
medicines to extend their shelf life or make them transportable
in the first place. Alongside vaccines, these include antibiotics,
serums, diagnostic agents, protein-based and biotechnological
products, cells, tissues and chemicals. Production must meet
the pharmaceutical industry’s exceptionally high quality and safety
standards. Many of the corresponding manufacturing processes are
traditionally energy-intensive. GEA significantly reduces this energy
requirement through its innovative systems and processes. The
company has been systematically expanding its capacities and capabilities
in this growth market for years.
GEA Group Aktiengesellschaft
D 40468 Düsseldorf
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For example, the topic of explainability of AI using heatmaps
can contribute to regulatory-compliant development.
© Fraunhofer IPA/Photo: Rainer Bez
Particularly, robotics in use without safety fences requires
special safety measures. © Fraunhofer IPA / Photo: Rainer Bez
Bringing AI legally compliant into
practice: Reallabor KIRR Real develops
exemplary AI and robotics solutions
The goal of »KIRR Real: Living Laboratory for Legally Compliant
AI and Robotics« of the Fraunhofer IPA and ARE-
NA2036 was to support companies in Baden-Württemberg
in implementing the EU AI Act as well as the EU Machinery
Regulation coming into force in 2027. The results of the collaboration
with 15 companies are now published and serve
as guidance for companies with similar applications to develop
AI and robotic systems in a legally compliant manner.
Time is of the essence when it comes to current regulations: On August
2, 2027, the obligations for high-risk AI systems as safety components
will come into effect, and the entire EU AI Act will apply.
The new EU Machinery Regulation also sets new requirements for
safety-related AI and self-learning systems starting in January 2027.
Regulatory and technical consulting for companies
KIRR Real helped companies understand and implement these
complex regulatory requirements. For this purpose, »Legal Quick
Checks« were offered, which are short, concise consulting projects.
A law firm classified these cases into one of the four risk classes of
the AI Act (from minimal to unacceptable risk). Subsequently, the
Fraunhofer Institute for Production Technology and Automation
IPA examined the technical documentation and underlying concepts
of the AI development to evaluate the legal compliance of the
systems and to develop practical recommendations.
The project ran from November 15, 2024, to December 31, 2025,
and was funded by the Ministry of Economics, Labour and Tourism
of Baden-Württemberg. The consortium consisted of Fraunhofer
IPA and the research campus ARENA2036, supported by several associated
partners. The main objectives of the project were to investigate
how well companies in Baden-Württemberg are prepared for
the AI Act and the Machinery Regulation, how the two regulations
interact and overlap, and where there are still hurdles in AI regulation.
The insights gained from the project provide impulses for practical
implementation and further development of AI regulation and
are actively fed back into the legislative process, for example through
participation in standardization committees, regular exchanges with
the Federal Network Agency, the Federal Institute for Occupational
Safety and Health, and a workshop with the Federal Ministry of Labour
and Social Affairs. The project results are also intended to influence
the design of the living labs provided for in the AI Act.
Raising awareness of regulatory requirements
During the project, 15 AI application cases from areas such as manufacturing,
humanoid robotics, healthcare, and personnel management
were addressed. Even companies with advanced AI development
still needed support in implementing the AI Act. Discussions
also revealed that awareness of upcoming regulations is often insuf-
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ficient. In applying the AI Act, either the legal or the technical aspect
was frequently considered, but both aspects and early engagement
with AI regulation are crucial for successful application.
Challenges in implementing the regulations
Particularly challenging for companies is the classification into risk
categories. This classification is crucial for resource planning but can
sometimes be ambiguous and depends heavily on the details of the
application case. Therefore, guidance based on similar cases is not
always possible.
The lack of harmonized standards means that more AI systems
must undergo conformity assessment by third parties. Regarding the
Machinery Regulation, many experts also see a need for clarification
on what exactly constitutes a system with »self-developing behavior«.
Another issue is the technical implementation of the requirements.
Many companies ask questions such as: How must evidence
be provided? How extensive must documentation be? When is AI
considered part of a machine? Handling multiple applicable regulations
is often unclear and causes fear of unnecessary additional
effort. Furthermore, many companies do not develop AI systems
entirely in-house but use existing general-purpose AI models for
their applications, which complicates the provision of the required
evidence. However, the available guidelines and support tools have
so far hardly addressed this practice.
An additional challenge for integrating AI into robots and other
machines is posed by the new Machinery Regulation: companies
must not only comply with the new rules for AI in safety functions
over the next twelve months but also adapt their existing products
to the new regulation.
Recommendations from the Living Laboratory
The experiences from KIRR Real show that while some companies
are engaging with the regulations, existing uncertainties, the multitude
of regulations to consider, and the lack of harmonized standards
pose significant problems.
There is an urgent need for concrete, practical, and easily implementable
guidelines, as well as structured approaches that start early
in development. Particularly, AI development teams—regardless of
company size—are often small and struggle to manage the required
efforts. Support offers (such as living laboratories) should therefore
be as accessible as possible to provide real added value. Companies
should also receive support early in development, for example
through legal assessments of an application case, workshops, or consulting
during system development.
The Fraunhofer IPA will continue to collect insights from the
project work and actively contribute to the legislative process, as well
as use these insights for direct collaboration with companies. Companies
can contact our representatives for this purpose. The goal remains
to further develop AI regulation in a practical manner and to
support companies in Baden-Württemberg optimally.
Fraunhofer-Institut für Produktionstechnik und Automatisierung IPA
Nobelstraße 12
D 70569 Stuttgart
Telefon: +49 711 970 1667
eMail: joerg-dieter.walz@ipa.fraunhofer.de
Internet: http://www.ipa.fraunhofer.de
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(Image credits: © nora)
(Image credits: © nora)
Noravant Timber Rubber Floors for Modern Laboratory and Cleanroom Architecture
When function creates atmosphere
Experts in laboratory technology and the planning of safety-related
facilities know: laboratories and cleanrooms are highly functional
work environments with clearly defined requirements. In recent
years, these requirements have continued to increase in an increasingly
complex environment. In addition to integrating innovative
technologies, adhering to strict safety standards, and optimizing
efficiency and resource utilization, aspects such as comfort, design,
and sustainability are now also coming into sharper focus. Atmosphere
and well-being are gaining importance – even in areas that
were long considered purely functional. This is precisely where the
new rubber flooring noravant timber comes into play. It combines
the appearance of natural wood design with the performance that
is indispensable in laboratories and cleanrooms. The sheet flooring
opens up new creative possibilities for areas where safety and design
go hand in hand.
between design and function is essential,“ says Bettina Haffelder,
Vice President DACH nora. „With noravant timber, it has
been possible to develop a flooring with an authentic wood look
that is easy to clean and characterized by outstanding resistance
to media.“
Durability for demanding applications
As important as aesthetics are – in laboratories and cleanrooms,
performance ultimately decides. The innovative surface technology
ensures an exceptionally high resistance against a wide range of laboratory
chemicals. This reduces cleaning effort and simultaneously
helps maintain the quality of the rooms in the long term – for a permanently
pleasant working environment and sustainable preservation
of the laboratory property.
Design as a functional added value
Colors, materials, and surfaces influence motivation, concentration,
and ultimately the quality of work results. The floor is
an integral part of modern laboratory architecture and plays an
important role within a comprehensive concept that considers
both function and design equally. The calm oak look of noravant
timber and its matte surface create a surface that intentionally
recedes and yet produces a pleasant room atmosphere. „Especially
in laboratory and cleanroom areas, the close connection
nora systems GmbH
Höhnerweg 2-4
D 69469 Weinheim
Telefon: +49 6201 2743934
Mobilfunk: +49 172 6330484
eMail: frank.baehr@nora.com
Internet: http://www.nora.com
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Invisible particles,
real consequences:
New Camfil film
shows why clean
indoor air protects
health
How clean is the air we breathe indoors, and what impact does it
have on our health? A film recently released by filter manufacturer
Camfil addresses these questions as part of the international series
„Healthier Together.“ Healthier Together is a series by the WHO
Foundation and was produced by BBC StoryWorks Commercial
Productions.
Whether cooking, heating, cleaning, or simply normal building
use: microscopic particles are generated in everyday life. In modern,
energy-efficient buildings, these particles remain in the air for a long
time if ventilation and filtration are inadequate – with consequences
for the well-being and health of the people inside the building.
„At Camfil, we work with something that cannot be seen, but
whose effects everyone can feel: air. Understanding and actively
controlling indoor air quality reduces risks, protects people, and
creates a noticeably better environment,“ says Anders Sundvik, VP
Product & Innovation at Camfil, who introduces the topic in the film.
Those responsible for schools, offices, and other public buildings
should not consider providing clean air merely as a technical issue,
but as an essential part of responsible building planning and management.
The film is available on the Camfil website. There, additional information
is provided on simple measures for better air quality at the
workplace.
About the series „Healthier Together“
Healthier Together is a video series created in collaboration with the
WHO Foundation. It was produced by BBC StoryWorks Commercial
Productions on behalf of participating organizations. The series
highlights global health challenges and opportunities – in cities and
villages, in hospitals and at home – and shows how people work together
to achieve the goal of health for all.
Camfil GmbH
Feldstr. 26 - 32
D 23858 Reinfeld
Telefon: +49 4533 2020
Telefax: +49 4533 202202
eMail: info.de@camfil.com
Internet: http://www.camfil.com
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Hermann Bantleon GmbH and IQM Oberflächentechnik GmbH
implement sustainable solutions for clean components
Holistic process optimization
in surface technology
Clean components are a central quality factor
in industrial manufacturing. Together
with IQM Surface Technology GmbH, Hermann
Bantleon GmbH has demonstrated
how demanding requirements in surface
technology can be efficiently and sustainably
implemented through a holistic view of
the entire process chain. From processing to
component cleaning to secure VCI packaging.
Goods carriers and components ready for
cleaning with Bantleon cleaning media.
(Copyright: Hermann Bantleon GmbH)
The starting point was the commissioning
of a new cleaning system at IQM. The challenge
was to find a partner for a cleaning
medium that can be used for all alloys offered
by the company to its customers – while
maintaining consistently high cleaning performance.
„With the commissioning of a new system
in 2021, we faced the task of finding a
cleaning medium suitable for all alloys we
process. At the same time, we had to ensure
that we reliably meet the high quality standards
of our customers,“ explains Sebastian
Trakies, Commercial Manager of IQM Surface
Technology GmbH. „With Bantleon, we
found this partner and can clean all components
in our cleaning system as needed
to ensure the quality of our customers on a
long-term basis.“
The focus of the project was to reliably
achieve clean components while optimally
coordinating all process steps. After
vibratory polishing, specially tailored cleaning
media ensure the effective removal of
contaminants. The subsequent residual dirt
analysis in a cleanroom guarantees compliance
with the required quality standards. In
this way, permanently clean components
and high process security for subsequent
manufacturing steps are achieved.
A key success factor was the individual,
technical consulting provided by Bantleon
throughout the entire process. In addition
to selecting the appropriate cleaning medium,
Bantleon also supported IQM in designing
the suitable VCI packaging. This
reliably protects the cleaned components
from corrosion and prepares them safely for
storage and shipping. Cleaning, corrosion
protection, and packaging were considered
as an integrated overall system and precisely
tailored to IQM‘s requirements.
„We especially appreciate that Bantleon‘s
technical advisor is always available
and supports us directly,“ says Melanie
Rehm, Production Manager at IQM Surface
Technology GmbH.
The joint success story shows that successful
cleaning and high-quality surface
technology do not arise from individual
products, but through partnership collaboration,
technical expertise, and a consistent
focus on the entire process. This way, quality,
efficiency, and sustainability can be increased
simultaneously – an approach that
is increasingly gaining importance in modern
surface technology.
Hermann Bantleon GmbH
D 89077 Ulm
The cleaning media from Bantleon
ready for use.
(Copyright: Hermann Bantleon GmbH)
VCI packaging by Bantleon for safe storage and secure transportation.
-(Copyright: Hermann Bantleon GmbH)
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Bild: AdobeStock_569552759
Synergies for high-tech
cleanroom planning
Lorenz Consult is now a partner in the Silicon Alps Cluster, an important technology
and innovation network for electronic and software-based systems in Austria.
As one of Austria‘s leading general planners for complex buildings, the company
is strengthening its network within the electronics and microelectronics industry.
The goal of the collaboration is to recognize technological trends early and integrate
them into the planning of highly specialized cleanroom infrastructures.
Focus on the Interface of Building and Process
The Silicon Alps Cluster brings together actors from industry, research, and the public
sector from southern Austria. For Lorenz Consult, this platform offers direct access
to the technological requirements of the future. Since cleanrooms in semiconductor
manufacturing or sensor technology are subject to extreme requirements for
particle-free environments, vibration isolation, and climate stability, close exchange
with system developers is essential.
„The partnership in the Silicon Alps Cluster provides us with a knowledge advantage.
We understand earlier how our customers‘ manufacturing technologies are
developing, and can precisely tailor the building infrastructure and building technology
accordingly,“ explains Christian Lorenz, Managing Director of Lorenz Consult.
Innovation and Sustainability in Cleanroom Technology
A central concern of the partnership is the consistent integration of technological
progress and sustainable building design. Especially in energy-intensive cleanroom
projects, resource and energy efficiency play a crucial role. Lorenz Consult uses the
network to further develop innovative planning approaches that meet the increasing
ecological and economic demands of the industry.
Strategic Added Value for High-Tech Industries
With this membership, Lorenz Consult consolidates its position as a specialized
partner for the electronics and microelectronics industry, as well as for pharmaceuticals,
laboratories/biosafety, and food. Customers benefit from planning that not only
meets current standards but also considers the technological cycles of the coming
years. The continuous transfer of process know-how from the cluster directly into
the planning phase ensures the future viability of demanding cleanroom and laboratory
projects.
Lorenz Consult Ziviltechniker GmbH
AT 8010 Graz
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Hannusch EMS Increases Line Flexibility
with ASYS Automation Solutions
Hannusch Industrieelektronik GmbH, based in Laichingen (Baden-
Württemberg, Germany), is an experienced EMS provider specializing
in demanding electronics manufacturing. To increase line flexibility
and optimize setup and throughput times, the company implemented
a new SMD production line equipped with automation and
software solutions from the ASYS Group. The collaboration between
Hannusch and ASYS has been ongoing since 2009 and was further
strengthened through this project.
Seamless Communication for Efficient Product Changeovers
The objective of the line concept was to economically manage up to
20 product changeovers per day without compromising equipment
availability or throughput. This required short setup times as well as
stable, standardized machine-to-machine communication across
the entire line.
The line is equipped with multiple ASYS modules for PCB handling,
including loading and unloading modules, transport systems,
buffer and magazine solutions, turning and singulation units, as well
as workstations and interface stations. The hardware is complemented
by the SynapticaOS Hermes Assistant as a central software solution
for product and line management.
The VEGO modules used automatically adapt to different PCB
formats and ensure a continuous material flow, even with frequent
product changes.
Scalable Architecture for Future Automation Steps
The Hermes standard and the associated software solutions are
continuously being further developed at ASYS. Currently, Hannusch
uses the Hermes Assistant for product data management and line
changeovers. Looking ahead, the changeover process is planned to
be further automated and executed directly at the machines. In addition,
cross-line communication is to be expanded in the future to
unlock further efficiency potential across the entire production environment.
“The collaboration was always very pleasant and on an equal
footing. Response times were fast, and the support was excellent.”
Michael Hannusch, CEO, Hannusch Industrieelektronik GmbH
Results and Added Value
– High line flexibility: Realization of up to 20 product
changeovers per day
– Standardized communication: Hermes protocol
as the foundation for scalability and future automation
– High equipment availability: Robust, low-maintenance ASYS
systems designed for continuous industrial operation
– Long-term partnership: Close, solution-oriented collaboration
with a focus on continuous process optimization
Successful Implementation of Standardized Interfaces
During the project, the integration of the Hermes standard posed
a technical challenge, as it is interpreted differently by various
equipment manufacturers. Through close coordination between
Hannusch, ASYS, and the involved machine suppliers, end-to-end
Hermes communication across the entire line was successfully implemented.
ASYS Prozess- und Reinraumtechnik GmbH
Lerchenbergstraße 31
D 89160 Dornstadt
Telefon: +49 7348 98560
eMail: cleanroom@asys-group.com
Internet: http://www.asys-group.com
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Arnt König takes over the operational leadership of the German market
– Group aligns management capacities more internationally
Testo Industrial Services expands
management team for further growth
Testo Industrial Services (TIS), one of the leading full-service providers in the
fields of measurement technology, quality management, and calibration in Europe,
is expanding its management team: Arnt König is appointed as the second
operational managing director and simultaneously takes on the role of Deputy
Managing Director from Raimund Föhrenbacher. With this step, TIS strengthens
its management structure and creates additional capacities for further international
growth and increasing demands within the group.
Führen das Unternehmen gemeinsam in die Zukunft: Raimund Föhrenbacher (rechts)
und der neue Geschäftsführer Arnt König (links). © Testo Industrial Services GmbH
Broad experience for key future tasks
velopment of the Swiss market and has
advanced international cooperation within
the group. His deep understanding
of customer needs, markets, and internal
processes makes him an ideal candidate
for the operational leadership of the
group‘s largest TIS market.
„For me, this new role is a great honor
and the next exciting development step,“
says Arnt König. „I look forward to further
expanding our strong market position in
Germany and actively shaping the group‘s
international orientation.“
In his new role, König will not only assume
operational responsibility for Germany
but also central customer-oriented topics
such as Sales & Marketing International – a
Arnt König brings an exceptionally broad
background of experience to his new role,
which has connected him closely with the
development of Testo Industrial Services
for over twenty years. Since joining in 2003,
he has actively supported and significantly
shaped the company‘s key growth phases.
His operational expertise ranges from sales-related
key positions to long-standing
leadership roles in the German organization,
up to international responsibility as Managing
Director of Testo Industrial Services
Switzerland.
In this position, König has provided
important impulses for the strategic dekey
to linking local excellence with global
strategy.
Strengthening of international
orientation
With the expansion of the management
team, Testo Industrial Services is focusing
even more strongly on the group‘s international
development. TIS has grown dynamically
in recent years and now works much
more closely with the national subsidiaries
and the parent company Testo in Titisee.
This environment necessitates a clear division
of roles to manage the increasing demands
of internationalization, scalability,
and synergies in a structured and futureoriented
manner.
Raimund Föhrenbacher will increasingly
focus on the strategic management of the
entire TIS group – particularly on implementing
the Group Strategy 2030 and establishing
stronger international collaboration.
The goal is to further increase the global
performance of the organization while specifically
strengthening operational focus in
the German market.
„Our group is growing rapidly, and with
it, the demands on leadership and internationalization,“
says Raimund Föhrenbacher.
„With the new structure, we create more
space for strategic development – and at the
same time ensure the necessary attention
for our strongest market in Germany.“
The new division of roles creates a clear
and efficient structure that optimally supports
both the international orientation and
the local market dynamics.
Testo Industrial Services GmbH
Gewerbestraße 3
D 79199 Kirchzarten
Telefon: +49 7661 909018000
eMail: gmp@testotis.de
Internet: http://www.testotis.de
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Green Elephant Biotech and
Bürkert Fluid Control Systems
present Archimedes® One for scalable
and automated adherent cell culture
Innovative partnership revolutionizes
cell therapy production
Green Elephant
Biotech presents
the dynamic adherent
bioreactor Archimedes®
One, a new platform
designed to simplify and
scale adherent cell culture
processes.
Green Elephant Biotech announced the introduction
of the Archimedes® One — Dynamic
Adherent Bioreactor, a new platform
designed to simplify and scale adherent cell
culture processes. The system was developed
in close collaboration with Bürkert
Fluid Control Systems, combining Green
Elephant Biotech’s cultivation technology
with Bürkert’s expertise in fluidic control
and automation. The collaboration between
the two companies began at analytica 2024,
when Bürkert’s application management
Joel Eichmann (left) and Felix Wollenhaupt (right) from Green Elephant Biotech, together with
Georg Stawowy (second from left) and Hendrik Faustmann (third from left) from Bürkert Fluid
Control Systems, proudly look back on their one-year partnership and their first joint product.
team discovered Green Elephant’s technology.
Recognizing the potential to jointly address
key challenges in biopharmaceutical
manufacturing, Bürkert subsequently joined
Green Elephant Biotech as a strategic investor,
establishing the foundation for a longterm
development partnership.
Together, the teams focused on integrating
advanced fluidic and automation technologies
with next-generation cell culture
systems. The result of this collaboration is
the Archimedes® One, the first system in a
new category designed specifically for scalable
adherent cell cultivation.
Adherent cell processes remain central
to many emerging cell and gene therapies
but are often difficult to scale. Traditional
two-dimensional culture systems rely on
manual workflows and large numbers of
vessels, while suspension systems frequently
require adapting sensitive cell types. Fixed-bed
bioreactors can provide scalability
but introduce significant hardware complexity
and operational overhead.
Archimedes® One takes a biology-first
approach. Instead of forcing adherent cells
into suspension or complex matrices, the
system enables controlled, perfusion-based
cultivation using the CellScrew® geometry,
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providing a large growth surface within a
compact footprint. Automated media distribution
and integrated cell harvesting reduce
manual intervention and support reproducible,
standardized workflows.
Through the integration of Bürkert’s
fluidic control technologies, the system
enables precise control of media and gas
flows. In combination with a connected
biocontroller, key process parameters such
as pH, dissolved oxygen, and temperature
can be monitored and controlled, bringing
bioreactor-level process control to adherent
cell cultivation.
“Cell therapy manufacturing should not
require choosing between biological integrity
and industrial scalability,” said Joel
Eichmann, Co-Founder of Green Elephant
Biotech. “With Archimedes® One, we are
introducing a platform that aligns process
control with adherent cell biology while significantly
reducing operational complexity.”
“The collaboration with Green Elephant
demonstrates how precise fluidics and
automation technologies can open up new
possibilities in cell culture technology,” says
Hendrik Faustmann, Manager New Business
Model Development at Bürkert Fluid
Control Systems. “By combining our expertise
in automation and system integration
with Green Elephant’s cultivation platform,
we have created a system architecture that
seamlessly integrates fluid management
and process control—optimally tailored to
the requirements of modern adherent cell
processes.”
The system is currently being introduced
to the market ahead of its planned commercial
launch later this year. In parallel,
Green Elephant Biotech is opening an Early
Access Program for selected cell therapy
companies and CDMOs, providing early
access to production units, dedicated technical
support, and the opportunity to contribute
to application data and case studies
ahead of the commercial launch.
“The Early Access Program allows us
to work directly with therapy developers
and CDMOs as we prepare for commercial
launch,” said Felix Wollenhaupt, Co-Founder
at Green Elephant Biotech. “Together,
we want to demonstrate how Archimedes®
One integrates into real manufacturing
workflows and supports scalable adherent
cell production.”
Green Elephant Biotech and Bürkert
Fluid Control Systems will present the dynamic
adherent bioreactor together at analytica
2026 in Munich (Stand A1.419), where
visitors can learn more about the joint development
and experience the system firsthand.
Companies interested in the Early Access
Program can apply via:
www.greenelephantbiotech.com/eap
Bürkert GmbH & Co. KG
D 74653 Ingelfingen
BioCapt® Single-Use Microbial Air Sampler
for a Continuous Cleanroom Monitoring
Learn more
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© Fraunhofer IPA/Foto Rainer Bez
»Humanoid Capabilities Navigator«:
What technical skills does a humanoid
robot possess?
A research team from Fraunhofer HNFIZ has published
a newly developed evaluation model that categorizes the
technical capabilities of humanoids across five levels of development.
Applications can also be classified based on the
robot capabilities required. The model makes humanoids
comparable, facilitates the selection of the right humanoid
for a specific application, and highlights open topics in
technology development.
Against the backdrop of increasing skilled labor shortages and rapid
advances in artificial intelligence (AI) and robotics, humanoid robots
are becoming increasingly prominent in industry and logistics.
Companies face the central question of when and for which tasks
humanoid robots are technically and economically viable or will
become so. Many companies and research institutions are already
testing initial systems, but until now, there has been a lack of a comprehensive,
comparable evaluation model.
Transparency and comparability for humanoid robots
This is where the Humanoid Capabilities Navigator, developed by
the Fraunhofer Institute for Production Technology and Automation
IPA at the Heilbronn site, comes into play. It has been published in a
newly released white paper. Fraunhofer IPA, as part of the research
and innovation center for AI-based robotics, is a component of the
Fraunhofer Heilbronn Research and Innovation Centers HNFIZ and
works on topics such as intelligent mobile manipulation and flexible
use of robotic arms, as well as humanoids.
The Humanoid Capabilities Navigator is broadly inspired by the
five levels of automation in autonomous driving and evaluates humanoid
robots based on four categories, which often include various
technical capabilities and their levels of development:
– Mobility and locomotion (including localization
and path planning)
– Manipulation (including force perception and grasp planning)
– Cognition (including perception and task planning)
– Safety and security
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For each capability within a category, humanoids can be classified
according to maturity levels from 0 (not present) to 4 (highly autonomous,
comparable to or better than humans). This allows for the first
time a transparent, manufacturer-independent, and well-founded
comparison of different humanoids and provides information about
their suitability for specific applications.
Practical assessment of real-world applications and robots
The publication illustrates the use of the Humanoid Capabilities
Navigator in typical industrial applications such as truck loading
and unloading, order picking, machine operation, and maintenance
tasks. For each task, the necessary technical maturity levels in
the four capability areas are outlined. For example, truck loading
demands the highest levels in manipulation, cognition, and safety,
while machine operation requires lower levels due to the more structured
process, which involves less flexibility in task execution.
Using a current humanoid robot, the G1 from Unitree Robotics,
the automation division of Fraunhofer IPA tested the Humanoid Capabilities
Navigator. It was found that the current G1 version has already
made significant progress in areas such as mobility. However,
there is still considerable development needed to fully meet industrial
requirements. The evaluation model makes these gaps transparent
and helps to specifically prioritize development efforts.
Guidance for research, development, and market forecasts
The Humanoid Capabilities Navigator provides industry with a practical
tool to realistically assess the potential of humanoid robots,
validate investment decisions, and derive targeted research and development
measures. It also enables a reliable assessment of future
market developments, as the progress of the technology is systematically
linked to specific application requirements.
This white paper is part of several publications that the institute
has already published or will publish in the first half of 2026.
All of them focus on providing companies with comprehensive
and reliable material to evaluate and assess the economic and
technical feasibility of deploying humanoid robots for their own
applications.
Fraunhofer-Institut für Produktionstechnik und Automatisierung IPA
Nobelstraße 12
D 70569 Stuttgart
Telefon: +49 711 970 1667
eMail: joerg-dieter.walz@ipa.fraunhofer.de
Internet: http://www.ipa.fraunhofer.de
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A-look-inside-imec‘s-300mm-cleanroom. (Photo: Imec)
Semiconductor-based
Quantum Pilot Line ‘SPINS’
launched with EU support
IMEC-SPINS. (Photo: Imec)
On April 2, 2026, SPINS (Semiconductor
Pilot line for Industrial Quantum NanoSystems)
was inaugurated, one of six European
quantum pilot lines. The consortium coordinated
by imec brings together 25 European
research institutions, industry partners, and
academic research groups to strengthen
Europe‘s leadership and sovereignty in this
strategically important field. The €50 million
SPINS pilot project is made possible
through co-financing from the European
Union‘s „Chips Joint Undertaking“ (Chips
JU) as well as national and regional authorities
of the participating member states.
Quantum computing has developed
into a highly strategic area with rapidly increasing
economic and societal importance.
Applications range from breakthroughs in
drug research and materials science to extremely
secure communication and nextgeneration
navigation systems.
However, there is still a gap between
current quantum research and the manufacturing
of quantum processors that enable
significant quantum applications. Scaling
the number of stable qubits (up to one billion)
is the key to building reliable and faulttolerant
quantum computers.
Considering the technological complexity,
which includes cryogenic operation,
high-precision control electronics, and
highly specialized manufacturing processes,
and given the strategic importance of quantum
chips, six complementary quantum
pilot lines have been established under the
EU-Chip Act. Each focuses on a specific
hardware platform and collectively advance
quantum technologies in the areas of quantum
computers, communication, and sensing.
Within this portfolio, SPINS is the pilot
line dedicated to semiconductor-based spin
qubits, with a primary focus on developing
quantum chips for quantum computer applications.
Imec coordinates this new pilot
line and leads a European consortium of 25
partners from research institutions such as
Fraunhofer, VTT, and CEA-Leti, from industry
(including large companies like Infineon
and Siltronic as well as SMEs and startups),
and from academic groups (such as TU Delft
and the University of Jyväskylä), who share
their knowledge and skills with the goal of
translating the strategic framework of the
EU-Chip Act into concrete actions.
Initial projects of the SPINS consortium
include process and design optimization
to create a robust foundation for scalable,
stable, and high-performance spin qubits
on three different technology platforms:
Si/SiGe, Ge/GeSi, and SOI. SPINS aims
to transfer this technology from the lab
into production via Multi-Project Wafers
(MPW) and standardized quantum Process
Design Kits (PDKs), lowering entry barriers
for startups and SMEs in semiconductor
quantum technology and laying the groundwork
for European companies to build early
quantum expertise.
Quote from imec - Kristiaan De Greve,
SPINS Coordinator: „Scaling qubits requires
an extremely controllable environment and
solid manufacturing processes due to the
extreme sensitivity of qubits to environmental
disturbances. These challenges demand
the precision and control only available in a
semiconductor cleanroom infrastructure, as
well as the research and innovation mindset
to adapt such environments to these sensitive
qubits. At imec, we have been creatively
tackling complex problems in modern semiconductor
manufacturing for over 40 years.
By pooling the expertise of our European
consortium partners in this quantum pilot
line, we will accelerate the development of
high-TRL semiconductor qubits and enable
quantum systems at a larger scale, made in
Europe.“
In addition to the semiconductor technology
pilot line, there are other European
quantum research projects, including the
photonics pilot line for quantum „P4Q“ (coordinated
by the University of Twente, NL),
in which imec is also involved; ion trap qubits
„CHAMP-ION“ (coordinated by SAL,
AT); superconducting qubits „SUPREME“
(coordinated by VTT, FI); diamond quantum
chips „DIREQT“ (coordinated by CNR, IT);
and neutral atoms „Q PLANET“ (coordinated
by Pasqal, FR).
IMEC Belgium
BL 3001 Leuven
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Production sites in Europe and the USA increase process efficiency and capacities
Vetter continues to expand his global
network for clinical manufacturing
– Construction measures at the new clinical site in Des Plaines
are proceeding on schedule
– Expansion of infrastructure at the Austrian site
strengthens clinical processes
– Established site in Skokie continues to show positive results
Vetter, one of the world‘s leading pharmaceutical
service providers in the field of
aseptic production of injectable medicines,
announces the further expansion of its global
network for clinical manufacturing. With
the continuous extension of its service offerings
in Vetter Development Service, the
company is taking decisive steps to provide
the necessary capacity, state-of-the-art
technologies, and specialized expertise to
meet the increasing worldwide demand. By
further strengthening its presence in Europe
and the USA, Vetter positions itself as a
reliable, long-term partner for biopharmaceutical
innovators worldwide.
“Our ongoing global expansion reflects
our holistic approach to comprehensively
support our customers in their clinical development,”
says Dr. Claus Feußner, Senior
Vice President of Vetter Development Service.
“Through investments in technology
and capacity, we provide our partners with
tailored manufacturing services for early development
phases, ensuring their molecules
successfully progress from the laboratory to
the clinic.”
US locations with strong performance
and major expansion projects
Vetter continues to grow in the USA. The
site in Skokie, Illinois, remains a key partner
for global biotech companies. Since its opening,
the site has supported over 140 customers
and more than 350 active substances
on the demanding path through clinical development.
Over 40% of Skokie’s customers
are startups or small companies with fewer
than 50 employees.
Building on this foundation, construction
of the new 15,000-square-meter facility
in Des Plaines, Illinois, is progressing on
schedule. With the steel structure expected
to be completed soon, interior work will begin.
After commissioning in 2029, the site
will further increase Vetter’s clinical production
capacities in the USA and strengthen
the company‘s long-term commitment.
The construction work at the Vetter
construction site in Des Plaines is
progressing as scheduled (April 2026).
©Vetter Pharma International GmbH
European site grows in response
to customer demand
Vetter’s European manufacturing facility in
Rankweil, Austria, is also developing very
positively in the production and quality
control of drug candidates for clinical trials.
To meet the steadily increasing project volume,
Vetter is implementing several infrastructural
adjustments at the site.
The measures include establishing an
additional weighing room and another formulation
area within the aseptic production
zone. Capacity for manual optical inspection
is also being increased. Additionally,
the service offerings at the site will benefit
from new cooling rooms, specialized freezing
units for API storage, and another incubation
chamber for microbiological testing.
Through continued process optimization
and capacity expansion on both sides
of the Atlantic, Vetter is strengthening its
role as a global partner for comprehensive
and cGMP-compliant clinical development
and aseptic manufacturing. Close coordination
between the European and US sites
ensures harmonized processes, consistent
quality standards, and the flexibility needed
to meet the evolving requirements of customers
worldwide.
Vetter Pharma International GmbH
D 88212 Ravensburg
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BASF and Schütz have signed a settlement agreement
for the construction of a highly automated production and
storage facility for Intermediate Bulk Containers (IBC) at BASF‘s
headquarters in Ludwigshafen. (Photo: Schütz)
Schütz invests in a state-of-the-art
IBC production facility at BASF’s
main plant in Ludwigshafen
– Construction of a highly automated production and storage
facility for intermediate bulk containers (IBC)
– Close proximity enables maximum delivery flexibility, short
transport routes and 24/7 just-in-time delivery
– Schütz’s investment underscores the strategic partnership
between the two companies
BASF and Schütz have signed an agreement
for the construction of a highly automated
production and storage facility for intermediate
bulk containers (IBCs) at the BASF
headquarters in Ludwigshafen. The new
IBC production facility will ensure the secure,
long-term supply of industrial packaging
to the BASF plant. Work on building the IBC
production facility is scheduled to commence
in the third quarter of 2026.
A supply concept firmly focused
on the future
Schütz has teamed up with BASF to develop
a new, comprehensive concept for the supply
of industrial packaging to the site, in the
course of which Schütz’s future production
facility and the chemical site will be closely
interlinked in terms of infrastructure and
logistics. A core component is the construc-
tion of a state-of-the-art IBC manufacturing
plant on a site directly adjacent to the
chemical company’s factory perimeter. The
concept also includes an advanced, digitalised
packaging warehouse that will be integrated
in the container production facility,
and the continued roll-out of the reuse, reconditioning
and recycling of used packaging
containers. “This project is not only a
bold signal for sustainable site development;
it also stands for highly-efficient, customerspecific
on-site solutions and the further
expansion of our role as a strategic partner
to the industrial sector”, says Roland Strassburger,
CEO of the Schütz Group.
“The targeted attraction of long-standing
partners and the investment in production
capacities close to the site create
decisive structural advantages for our main
plant”, says Helmut Winterling, President
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creates maximum supply security for our
operations. The proximity and integration
keep transport routes short and allow us to
respond flexibly at all times to changing demands
in our production plants and facilities”,
says Uwe Lohr, Senior Vice President
Global Indirect Procurement, BASF SE.
A partnership spanning decades
provides a solid foundation
Schütz has developed a new, comprehensive supply concept with industrial packaging
for the Ludwigshafen site in collaboration with BASF. A core component is the establishment
of a state-of-the-art plant for IBC manufacturing on a site owned by the chemical company,
located in close proximity to the Verbund site. (Photo: Schütz)
European Verbund Sites, BASF SE. “The
integration of IBC manufacturing into our
material and production cycles strengthens
our competitiveness in the long term.”
“Schütz’s new site close to our facility
The collaboration between BASF and
Schütz dates back to the 1960s. A milestone
was the development of the world’s first IBC
in 1975 by Udo Schütz in close cooperation
with BASF – an innovation that fast became
the standard for industrial packaging
worldwide. At the BASF site in Ludwigshafen,
the classic intermediate bulk container
is used, among other things, for the storage
and transport of chemical products in liquid
form; these typically include chemical
bases such as dispersions, additives and
surfactants. Today, Schütz operates a global
production network with more than 70 locations
and supplies BASF sites worldwide as
well as numerous other customers across a
wide range of industries.
SCHÜTZ GmbH & Co. KGaA
D 56242 Selters
Clean Room Design
Glatt Process & Plant Engineering
Pharma+Biotech provides a
holistic planning that brings
together all interfaces and
engineering disciplines in
advance.
Cleanrooms as an integral part of
complex system planning.
Let‘s develop your
optimum solution.
ppe.glatt.com
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Analytik Jena celebrates
40 years of Biometra
– a success story in
molecular biology
Analytik Jena, together with its subsidiary Biometra, looks
back on four decades of technological excellence in molecular
biology. Since its founding in 1985, Biometra has significantly
influenced laboratory practices – from early electrophoresis
systems to pioneering PCR thermocyclers and
modern platforms for automated, precise workflows. This
success story is closely linked to customer proximity, engineering
craftsmanship, and a clear quality standard.
In the early years, Biometra relied on precision and reliability: the
first products enabled efficient separation and analysis of DNA,
RNA, and proteins. They quickly became standard in many laboratories.
The introduction of early PCR thermocyclers in 1989 marked
a turning point: DNA amplification became faster, more precise, and
user-friendly. In the 1990s, Biometra established its role as a trusted
technology partner in research and diagnostics worldwide.
In the 2000s, Biometra strategically expanded its portfolio:
solutions for DNA/RNA extraction and quantitative PCR (qPCR)
were added to meet the growing demands of modern laboratories.
A milestone in the company‘s history followed on May 11, 2009:
Biometra became part of the Analytik Jena Group. This connection
strengthened the joint product offering – from thermocyclers to
electrophoresis and blotting to imaging and hybridization technologies
– and opened new markets as well as synergies in development
and service.
The impact on science and society is well documented: with
the TGradient thermocycler, Biometra contributed to decoding the
human genome, a milestone in modern biology. During the CO-
VID-19 pandemic, the central importance of (q)PCR systems was
reaffirmed: Biometra technologies supported molecular diagnostics
worldwide at a high level. Strategic collaborations – for example with
Max Planck institutions in protein purification – further promoted
knowledge exchange and accelerated innovations that resulted in
practical solutions.
Since the 2020s, Biometra has increasingly focused on energy
efficiency, sustainability, and integration into automated laboratory
environments – always with the goal of making precise results available
faster and more robustly.
“Our vision is to shape the next 40 years as boldly and consistently
as the past ones,” says Eggert Appel, Head of Product Development
at Biometra. “Technologically mature products, high userfriendliness,
and seamless integration into automated processes
remain central guiding principles of our work.”
Oliver Klaeffling, Managing Director of Analytik Jena GmbH +
Co. KG, thanks all employees, partners, and customers who have
accompanied Biometra over four decades. “Your commitment and
trust are the foundation of our success – and an incentive for the
future.”
Analytik Jena GmbH+Co. KG
D 07745 Jena
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Dr.-Ing. Carlos Paiz Gaitca, Business Owner Industrial Analytics (left)
and Ralph Scheller, Team Leader of Software Development
at ResMa (right), accept the award. Image source: Weidmüller
ResMa® monitors the values from numerous
measurement stations and offers visualization options.
Image source: Weidmüller
Award for Energy Management
and Regression Analysis
The resource and energy management system ResMa® from Weidmüller
has been awarded the Product of the Year by Industrial Production.
The system achieved third place in the category „Energy
Technology and Electromechanics.“ The award „recognizes outstanding
industrial products and projects,“ according to the self-description.
ResMa® steps onto the winners‘ podium. At the official award
ceremony of Industrial Production in Munich, the energy management
system was chosen for third place in the category „Energy
Technology and Electromechanics.“
The approach of ResMa® was recognized for not only transparently
evaluating energy consumption using regression and
correlation analyses but also reliably predicting it. By normalizing
historical and current data, savings can be objectively assessed
and future consumption realistically forecasted — independent of
external influences such as temperature or working hours. „The
award is a great honor and shows that our products meet the
needs of our customers and the requirements for more efficient
energy use,“ reports Dr.-Ing. Carlos Paiz Gatica, Product Owner
for Industrial Analytics.
The jury for the award consists of the readers. In an open online
voting, they can vote for their favorites. Ralph Scheller, Team Leader
of Software Development for ResMa®, is also excited: „I am pleased
with the great appreciation from the readers. A special thanks goes
to the team that has worked long and intensively on ResMa® and
continues to do so every day.“
ResMa® is a browser-based software that centrally collects all
energy and production data via various interfaces. With its extensive
analysis and visualization functions, it enables far more than traditional
energy management, as users also gain detailed insights into
workflows and production processes. This helps ResMa® not only
monitor energy but also specifically improve the efficiency and quality
of operational processes.
The software combines energy management with comprehensive
evaluation, analysis, and visualization options — as a tool for process
optimization and their energetic requirements. Based on detailed
knowledge gained about processes and energy flows within the
company, potentials can be identified to optimize processes.
ResMa® also supports compliance with the requirements of the
Energy Efficiency Act, prepares CO₂ balances according to CSRD,
and systematically implements energy management according to
DIN EN ISO 50001. This creates a reliable data basis for more efficient
processes and regulatory security.
Weidmüller GmbH & Co. KG
D 32758 Detmold
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Seite 41/73
c/o Analytik Jena
Analytik Jena supports again as a sponsor
Bunsen-Kirchhoff
Prize 2026 awarded
at analytica
At the analytica conference, the renowned
Bunsen-Kirchhoff Award for Analytical
Spectroscopy was presented on March 26,
2026. Analytik Jena is pleased to support
this long-standing, internationally esteemed
award again this year as a sponsor and
to promote the laureate with a prize money
of 3,000 euros.
The Bunsen-Kirchhoff Award is awarded
by the German Working Group for Analytical
Spectroscopy (DAAS) of the German
Chemical Society (GDCh) and recognizes
outstanding scientific achievements in the
field of analytical spectroscopy. It is one of
the most important recognitions for excellent
research in this field and is a central
component in promoting young scientists
in the advanced stages of their careers.
Prof. Dr. David Clases receives
the Bunsen-Kirchhoff Award 2026
This year, the award goes to Prof. Dr. David
Clases, University of Graz. He has distinguished
himself with his work in the field of
Element Mass Spectrometry, particularly
ICP-TOF-MS (inductively coupled plasma
time-of-flight mass spectrometry).
Prof. Dr. Clases is internationally regarded
as one of the most innovative young
researchers in analytical spectroscopy. His
research at the interface of ICP-MS, nanostructure
analysis, and hybrid measurement
methods has gained significant global attention
in recent years.
His groundbreaking contributions include,
among others:
- Further development of high-resolution
ICP-TOF-MS, enabling the simultaneous,
rapid, and highly accurate analysis of
complex particle systems.
- Multimodal approaches that combine
ICP-MS with complementary methods
such as optical trapping or Raman
spectroscopy – a crucial step toward
capturing both elemental and molecular
information in a single measurement.
- Significant advances in particle
characterization, relevant for
environmental analysis, materials
research, and biomedical questions.
With more than 70 publications, numerous
international awards – including the JAAS
Emerging Investigator Lectureship 2025 –
and a highly visible presence in scientific
committees and conferences, Prof. Dr. Clases
is considered a “Rising Star” in spectroscopy.
Judging Committee’s Statement
The DAAS judging panel, composed of representatives
from universities, research
institutes, and industry, sees a particularly
high scientific and technological added value
in Prof. Dr. Clases’s work. His research
significantly contributes to further developing
ICP-TOF-MS technology – a techno-
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logy that, thanks to its multi-element capability
and coupling options, is regarded
as a key technology for future laboratory
analysis.
Opinions from the Scientific Community
Prof. Dr. Carsten Engelhard, Chairman of
DAAS and chair of the Bunsen-Kirchhoff
Award jury, emphasizes the importance of
the award:
“The Bunsen-Kirchhoff Award has a
long tradition and is highly regarded both
nationally and internationally. It recognizes
exceptional scientific achievements in analytical
chemistry, from optical spectroscopy
to mass spectrometric analysis. The work of
Prof. Dr. Clases is outstanding in its scientific
depth and practical relevance and possesses
high transfer potential for industry,
environmental, and materials analysis.”
Analytik Jena once again as a supporter
of scientific excellence
Analytik Jena is proud to have supported
the Bunsen-Kirchhoff Award for many years
and to contribute to promoting innovative
analytical research.
“The scientific insights recognized by
this award shape the further development of
analytical methods worldwide. As a technology
provider, we see it as our responsibility
to make cutting-edge research visible and to
support young scientists,” said Oliver Klaeffling,
Managing Director of Analytik Jena
GmbH+Co. KG.
About the Bunsen-Kirchhoff Award
The award is presented every two years and
targets outstanding researchers in the field
of analytical spectroscopy. It traces back to
a decades-long tradition within the GDCh
Working Group for Analytical Chemistry
and was first awarded in 1990. The ceremony
takes place during the analytica conference
in Munich.
Analytik Jena GmbH+Co. KG
D 07745 Jena
WIR MESSEN
NACH NORMEN
ISO 14644
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ANNEX 1
MEDIZINISCHE DRUCKLUFT
UND WEITERE EDELGASE
ISO 8573 + PHARMACOPEIA
C-tec Cleanroom-Technology GmbH
Tübinger Straße 47 D 72127 Kusterdingen
Tel.: +49 7071 6887180 Fax: +49 7071 688718700
E-Mail: public@c-tec.de www.c-tec.de
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Fraunhofer ISIT strengthens its expertise in microfabrication:
Prof. Dr. Erica Lilleodden takes over the leadership
of the Microfabrication Processes business unit. The
materials scientist brings international experience from
research and institute management. At ISIT, she develops
manufacturing processes for microstructured systems and
microelectronics. The goal is to bring innovative microfabrication
faster into industrial applications and to strengthen
Europe‘s technological sovereignty.
New impulses for industrial
micro-manufacturing:
Prof. Dr. Erica Lilleodden heads
the business unit at Fraunhofer ISIT
The Fraunhofer Institute for Silicon Technology ISIT is strengthening
its expertise in microfabrication: Prof. Dr. Erica Lilleodden has
taken over the management of the Microfabrication Processes business
unit. With her international research experience and extensive
leadership expertise, she will drive the strategic development of this
central technology area.
Microfabrication as a key technology
for the next generation of microsystems
The Microfabrication Processes business unit is one of the largest
and most technologically central areas at Fraunhofer ISIT. The focus
is on developing and optimizing processes for the production of microstructured,
multi-material systems – especially for applications in
microelectronics and adjacent future fields.
„This business unit addresses the industrial requirements for
new manufacturing approaches for microstructured components
and systems,“ explains Lilleodden. „Our work benefits significantly
from close integration with other business units as well as from direct
access to the cleanroom infrastructure at the institute.“
International expertise meets applied research
Prof. Dr. Erica Lilleodden is an internationally experienced materials
scientist with positions in the USA and Germany. After earning her
doctorate at Stanford University, she worked at leading research institutions
such as Lawrence Berkeley National Laboratory and Sandia
National Laboratories.
In Germany, she shaped materials research for many years at the
Helmholtz-Zentrum Hereon and as a professor at the Hamburg University
of Technology. Most recently, she served as director of the
Fraunhofer Institute for Microstructure of Materials and Systems
IMWS in Halle (Saale).
With her move to Fraunhofer ISIT, she consciously combines
a change in perspective: „The role as business unit leader enables
much closer collaboration with scientists and industry partners on
an operational level,“ says Lilleodden. „I want to actively shape the
scientific strategy and especially expand the testing and diagnostics
area.“
Focus on process understanding, functionality, and reliability
A central differentiator of ISIT, according to Lilleodden, is the holistic
view of microfabrication processes: „We not only develop processes
but also identify new functionalities and specifically investigate
the reliability of the resulting systems,“ she says. „Diagnostic methods
play a crucial role here – especially to understand why components
work or don‘t.“
Response to increasing demands from industry and society
The requirements for microsystems are constantly growing – driven
by technological, economic, and societal developments.
„The pressure to innovate is enormous,“ emphasizes Lilleodden.
„Systems must be more powerful, sustainable, and at the same time
cost-efficient. These demands often stand in direct tension with
each other.“
Fraunhofer ISIT addresses these challenges through application-oriented
research and close cooperation with industry partners.
The goal is to align technologies early on with industrial requirements
and to transfer them efficiently into application.
Strategic role for microelectronics and European sovereignty
A particular focus is on strengthening microelectronics in Germany
and Europe. In the context of the Microelectronics Germany
research factory (FMD) and European initiatives like the EU Chips
Act, Lilleodden sees great opportunities for ISIT: „We will increa-
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Seite 44/73
singly work on complex issues that are crucial for Europe‘s technological
sovereignty – for example, in prototype development, process
optimization, and wafer-level packaging,“ she says.
Leadership with a focus on collaboration and development
In her new role, Lilleodden relies on teamwork, interdisciplinary
exchange, and targeted support for young talent: „Everyone in the
team contributes with individual skills to overall success. It is crucial
to recognize these strengths and develop them together,“ she says.
She places particular importance on combining scientific excellence
with practical application: „Research at Fraunhofer means
translating knowledge into solutions that work in practice.“
Clear vision: technological leadership in microfabrication
For the coming years, Lilleodden has a clear goal: The Microfabrication
Processes business unit should be positioned as a leading
partner for innovative manufacturing technologies – nationally and
internationally.
„Our contribution to microelectronics is decisive,“ she summarizes.
„We develop technologies that enable future applications – from
AI to quantum technologies to medical sensors.“
Fraunhofer-Institut für Siliziumtechnologie ISIT
D 25524 Itzehoe
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Independent award cements Vetter‘s position as a leading CDMO
Vetter awarded as winner at
the CDMO Leadership Awards 2026
– Important Industry Recognition for CDMOs
– Selection based on quantitative metrics and
verified reviews from the biopharma industry
– The award emphasizes the trust of the industry
and customers in Vetter
Vetter, a globally operating service provider for pharmaceutical and
biotech companies specializing in the manufacturing of essential
and life-enhancing medicines, receives the CDMO Leadership
Award 2026 as CDMO of the Year in the „Finished Dose“ category.
The award honors companies that stand out through exceptional
achievements in engagement, quality, and technical expertise, and
underscores Vetter‘s role as a reliable partner for the biopharma industry.
The award winners were announced during DCAT Week on
March 25, 2026, in New York.
“Our goal is to support our customers in the long term and according
to their needs,” says Lars Hahn, Senior Vice President of Global
Sales Organization at Vetter. “The award confirms our focus on the
highest quality, reliability, and collaborative partnership. Above all, it
recognizes the work of our more than 7,300 employees worldwide.”
Investments in Capacities and Technologies
The award reinforces Vetter’s important role as a strategic partner
in the development and manufacturing of injectable medicines.
The pharmaceutical service provider supports its customers across
the entire value chain, from process development through clinical
and commercial filling to a wide range of assembly and packaging
services. In light of continuously increasing demands on the manufacturing
processes of complex biological medicines, Vetter is expanding
its capacities, technological expertise, and quality systems:
Strategic investments in Europe and the USA strengthen the global
development and production infrastructure. Overall, the company
plans investments of around two billion euros by 2035.
Reputable Industry Award with Independent Data Basis
“The CDMO Leadership Awards represent much more than mere
recognition,” says Louis Garguilo, Editor-in-Chief of Outsourced
Pharma. “They reflect direct feedback from clients as well as the
practical experiences of companies that must succeed in an increasingly
complex development and production environment. The finalists
and winners this year have convincingly demonstrated that
they deliver reliably, continuously adapt to new requirements, and
act as trustworthy partners.”
The CDMO Leadership Awards are awarded annually by the media
group Life Science Connect and the trade publication Outsourced
Pharma and are among the prestigious industry awards. The basis
for the award is an independent study by the Boston-based Tufts
Center for the Study of Drug Development, which is based on quantitative
performance data and verified reviews from pharmaceutical
and biotech companies.
Vetter Pharma International GmbH
D 88212 Ravensburg
The Vetter team proudly accepts the award (from left): Dr. Sebastian Schuck, Vice President of Key Account Management, Lars Hahn, Senior
Vice President of Global Sales Organization, Ayse Hizli, Vice President of New Business Development, Michele Cavalheiro, Key Account Manager,
and Dr. Claus Feussner, Senior Vice President of Development Service. © Vetter Pharma International GmbH
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Own subsidiary for the Spanish market
ENGEL Spain strengthens customer
proximity, service and access
to technology in Spain
With the rebranding of its former sales partner Roegele as ENGEL Spain, injection
moulding machine manufacturer ENGEL is expanding its direct presence in
the Spanish market. Since 1 April, the company has been represented in Spain by
its own subsidiary. For local plastics processors, this combines the continuity of
a team established on the ground for decades with direct access to the technology,
service and solutions portfolio of the global ENGEL Group – from injection
moulding machines and automation to digital assistance systems. ENGEL now
has its own subsidiary in the Spanish market.
Local continuity and global support
structures
Since 1972, Roegele has supported customers
in Spain in sectors such as automotive,
packaging, medical and technical moulding,
providing sales, service, training and consultancy
relating to ENGEL injection moulding
solutions. Building on this long-standing
partnership, the injection moulding
machine manufacturer is now taking the
next logical step. With ENGEL Spain, customers
will continue to work with the same
trusted contacts and benefit from the same
local market expertise. Service and application
engineering expertise will be integrated
even more closely into the corporate group’s
international network.
“The integration into the ENGEL Group
strengthens our local presence in Spain and
enables us to offer our customers even better
service and technical support,” says Daniel
Vizuete, Managing Director of ENGEL
Spain.
Barcelona site to be expanded
ENGEL is making targeted investments in
local structures, application engineering
and service capacity in Spain. At the Barcelona
site, a technical centre for training and
a showroom are being established. This will
strengthen ENGEL Spain’s local technical
support and shorten service response times.
For customers, the combination of local presence
and global connectivity will become
even more immediately accessible.
“With ENGEL Spain, we are creating
the conditions to support our customers in
the Spanish market even more directly and
to further develop our local presence in a
targeted manner,” says Benjamin Lettner,
VP Europe West & East. “In doing so, we are
building on long-established customer relationships
and an experienced local team.”
Broad portfolio for the Spanish market
Spain is one of Europe’s key plastics markets
and an important market for ENGEL in
south-western Europe. ENGEL has traditionally
had a strong presence here in the automotive
industry; at the same time, packaging
and the second brand WINTEC offer
further potential. For processors in Spain,
this expands access to solutions that are
both commercially and technically suited to
a wide range of market requirements. This
offering will also be showcased at Equiplast
in Barcelona in early June: ENGEL Spain will
present exhibits from the automotive, packaging
and technical moulding sectors, including
a tie-bar-less victory 120 with viper
20 linear robot, the all-electric e-mac 200
and e-motion 220, as well as the WINTEC t-
win 6500. The trade fair presentation will be
complemented by digital assistance systems
and connected production solutions.
Daniel Vizuete, Geschäftsführer ENGEL Spain
(Bild: Engel)
Benjamin Lettner, VP Europe West & East
(Bild: Engel)
ENGEL AUSTRIA GmbH
AT 4311 Schwertberg
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The research group of Prof. Dr. Peter Neubauer combines robots, analysis devices,
and artificial intelligence into effective research teams
A laboratory without people
It sounds a bit like science fiction: a laboratory that can plan, conduct,
and evaluate its experiments largely independently. In which
computers and artificial intelligence (AI) control robots work together
with state-of-the-art analysis devices. And in which no human
has to burn the night hours feeding cells and keeping experiments
running. But exactly that has become a reality at the KIWI Biolab
at TU Berlin. The developers of the fully automated high-tech laboratory
will also make their know-how available in the new research
center „The Simulated Human“ (Si-M) of TU Berlin and Charité –
Universitätsmedizin Berlin.
„I‘ve always been interested in how to bring new biological processes
from the lab into practice as quickly as possible,“ says Prof. Dr.
Peter Neubauer, who heads the Department of BioProcess Engineering
at TU Berlin. The co-founder and director of the KIWI Biolab
is a trained microbiologist. So he initially asked himself questions
mainly regarding bacteria, yeasts, and fungi: How can such organisms
be best kept in bioreactors? In a way that they not only reproduce
and thrive well but also produce valuable substances, such as
specific proteins for the pharmaceutical industry?
Finding an answer to this is anything but easy. Because these
tiny manufacturers often react very strongly to their environment. In
a laboratory experiment at the milliliter scale, they may behave perfectly.
But that doesn‘t necessarily mean they will do the same in a
bioreactor with several hundred cubic meters of content. Therefore,
before industrial use, it is essential to determine under which conditions
which organisms can best perform the desired task.
Automated work in the laboratory
Model calculations can provide clues. How quickly does an organism
grow? How much substrate does it consume? Peter Neubauer and
his team compile these and many other parameters into mathematical
formulas. In the computer, different process variants can then be
compared to see which one yields the best results.
„But we can also connect such mathematical models with robots
and analysis devices,“ explains Peter Neubauer. In this way, work in
the lab can be organized and automated digitally. One type of robot,
for example, sucks a few milliliters of liquid from the bioreactor
at specific times. One of its mobile colleagues then transports the
sample to a measuring device that analyzes its properties. For this to
work, the technical helpers must coordinate their work so that each
does the right thing at the right moment. „For this, we need extensive
computer programs,“ says Peter Neubauer.
Extremely interesting for the pharmaceutical industry
But the effort is worth it. The KIWI Biolab is now one of the world‘s
leading laboratories for the development of bioprocesses. Through
the use of mathematical models and artificial intelligence, even
At KIWI Biolab, one of the world‘s leading laboratories for the development
of bioprocesses, a 48-bioreactor system integrated into a laboratory
robot is used, enabling the parallel cultivation and automated monitoring
of biological processes under controlled conditions.
complex experiments can be carried out fully automatically. The AI
decides, for example, when it makes sense to take a sample and then
initiates the necessary steps. It ensures that the organisms in the
bioreactor lack nothing, automatically maintaining temperature, pH,
and other influencing factors in the optimal range. This way, it controls
the process so that it delivers the maximum yield or a specific
quality of the desired product. It even recognizes when an experiment
is not going well, so it can be aborted, repeated, or modified.
„All of this is, for example, extremely interesting for the pharmaceutical
industry,“ says Peter Neubauer. Is it worthwhile to move
from the lab to application with a new product? Which of several
possible candidates is the most promising? And what will the optimal
process for production look like later? Such questions can be
answered much faster and more efficiently in the KIWI Biolab than
in a conventional laboratory.
Data marketplace for the biotechnology industry
No wonder, then, that Peter Neubauer and his team collaborate with
many pharmaceutical manufacturers on various projects. „Developing
a new drug costs an average of 2.5 billion US dollars and takes
ten to fifteen years,“ the researcher says. Every superfluous experiment
and every saved day benefits patients and companies alike.
From industry, a new challenge was also posed to the TU group.
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„So far, we‘ve mainly dealt with processes involving microorganisms,“
explains Peter Neubauer. „But there is also great interest in
similar procedures for cell cultures.“ His working group will focus on
this in the future at the Si-M research center, where TU Berlin and
Charité – Universitätsmedizin Berlin cooperate.
Another focus will be the development of a data marketplace for
the biotechnology industry: What information must be recorded during
an experiment to ensure it can be reproduced? How should the
data be presented and offered to others so that they can understand
and utilize it? The team has gained extensive experience in such
questions over the years.
„From my point of view, we are not a core group at Si-M,“ the
scientist clarifies. Therefore, only a small part of his team will gradually
move to the new research center. „But our expertise is interesting
for many groups working there.“ Because robots and AI are likely to
play an increasingly important role in other laboratories in the future.
And to ensure that the technical research helpers do what they are
supposed to, much work remains for Peter Neubauer and his team.
The Research Center „The Simulated Human“ (Si-M)
On April 22, 2026, four years after groundbreaking, the doors of the
five-story research building „The Simulated Human“ will open. On
the campus in Berlin-Wedding, medical professionals, natural scientists,
and engineers from many disciplines of TU Berlin and Charité
– Universitätsmedizin Berlin will work closely together to develop
new therapeutic and diagnostic approaches for diseases. Bioanalytics,
organoid technologies, and methods for cell measurement are
intertwined with single-cell genetics, bioinformatics, automation,
and medical technology, often combined with other fields and excellence
clusters. Artificial mini-organs from human cells, fitting on
a chip, are intended to replace animal testing; by stitching together
interacting proteins, previously unknown processes in cells will become
visible.
Architecturally, the Si-M building already reflects the integrated
working atmosphere and the planned dialogue with the public: In
the light-filled central atrium with a café and a round lecture hall, an
impressive open staircase spirals upward. It leads to spacious laboratories
equipped with advanced technology such as mass spectrometry,
bioprinting, laser scanning microscopy, and others.
Further information:
The Department of Medical Biotechnology will also be represented
at the new Berlin research center „The Simulated Human“ with its
organoid research. Read here about the research of Prof. Dr. Sina
Bartfeld.
Technische Universität Berlin
D 10587 Berlin
Conveyor belts ensure a steady flow of materials in the medical technology sector and meet the
highest requirements for purity, precision, and integration into automated processes.
Conveyor belts in medical technology:
Precision and purity in focus
In medical technology, conveyor belts are a central component of
safe and stable production processes. They enable a consistent material
flow and help reduce errors and contamination risks.
Manufacturers face high demands: cleanroom compatibility,
ESD safety, vibration-free processes, and seamless integration into
automated systems are crucial. At the same time, conveyor belts
must be easy to clean and reliably protect sensitive components.
Montech offers specialized conveyor belt solutions that combine
precise transport, compact designs, and high reliability. Systems
like TB30 and TB40 enable exact positioning, stable workflows, and
flexible integration into various applications – from assembly to packaging
of sensitive products.
Efficient conveying technology for the high-precision medical industry.
(Copyright: MONTECH AG)
Montech AG
Gewerbestrasse 12
CH 4552 Derendingen
Telefon: +41 326815500
eMail: info@montech.com
Internet: https://www.montech.com
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Final report — Growth in visitor numbers,
full halls, clear future topics:
analytica 2026 sets standards
– 1,135 exhibitors from 40 countries
– About 35,000 visitors from 115 countries
– AI and automation as innovation drivers for the industry
Full halls, more visitors, highly satisfied exhibitors: analytica
2026, held in Munich from March 24 to 27, impressively
demonstrated how innovative and forward-looking the
international laboratory industry is. 1,135 exhibitors from
40 countries presented their world premieres and new products
from the entire spectrum of laboratory technology,
analysis and biotechnology to about 35,000 visitors from 115
countries. Conversations at the stands and in the supporting
program were all about the digital, automated, and sustainable
laboratory—and mostly the hot topic of AI.
“With a noticeable increase in the number of visitors and exhibitors,
and a high share of international participants, analytica 2026 confirmed
its status again as a world-leading trade fair,” says Dr. Reinhard
Pfeiffer, CEO of Messe München. “It once again made the dynamism
and innovative strength of an industry visible that supplies the
essential basics for growth fields such as food and quality control, life
sciences, and environmental technology.”
“analytica 2026 consistently addressed the most important industry
topics in the exhibition area, at the conference, and in the
supporting program. That makes it a unique platform for making
trends tangible, imparting specialist knowledge, and providing
orientation for the future of the laboratory,” adds Exhibition Director
Approximately 35,000 visitors from 115 countries attended analytica 2026.
© Messe München GmbH
Susanne Grödl. “The positive response from exhibitors and visitors
shows that we struck a chord with that and provided important impetus
for the industry.”
Exhibitors report very positive outcome
The exhibitors were very satisfied with the trade fair and were often
continuously involved in discussions at the stands. Dr. Gunther
Wobser, Managing Partner of Lauda Dr. R. Wobser and new Chairman
of the analytica Advisory Board, sums up: “analytica 2026 impressively
reaffirmed its status as the most important international
meeting place for the industry.” For Sylveer Bergs, Managing Director
Thermo Fisher Dreiech, analytica is the platform which unites all
industry stakeholders: “It showcases high-end analytics, integrated
life science workflows, digital and automated labs, and sustainable,
regulated applications, reflecting the move from standalone instruments
to connected, data-driven end-to-end solutions.”
Mathis Kuchejda, Managing Director of Schmidt + Haensch and
Chairman of the Analytical, Bio and Laboratory Technology Division
at the industry association Spectaris, adds: “Despite a challenging
market environment in recent times, there is a mood of optimism in
the industry—underpinned by the high level of innovative strength
and positive prospects in the long term.” Experts anticipate an annual
growth rate of five percent for the global laboratory market in the
next few years. This development is being driven primarily by automation,
robotics, and rising investments, for example, in life sciences,
pharmaceutical research, and environmental analysis.
Major attractions: special shows on the modern lab
The usual extensive supporting program addressed hot topics in
the industry and made them accessible in lectures, discussion panels,
and special shows. The daily live demonstrations, such as the
Special Show Digital Transformation, were a major attraction. Organizer
Felix Lenk, CEO of SmartLab Solutions, is extremely positive
about how things went: “You could feel the enthusiasm of the trade
fair visitors not only during the live demonstrations but also in the
hundreds of individual conversations about AI, digitalization, automation,
and robotics.” Nearby in the Live Lab, the rows of seats for
spectators were also full several times a day when experts presented
typical work processes from modern everyday laboratory life. The
experimental presentations in the Lab Safety Forum, which illustrated
the risks involved in laboratory work complete with bangs and
smoke, were also popular. The Jobday on the last day of the trade fair
drew large crowds. It offered graduates and young professionals the
opportunity to find out about professional prospects in the industries
and get to know potential employers.
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Scientific exchange at the highest level
There was intensive specialist discourse at the accompanying scientific
conference, which had over 2,000 participants. “Analysis is the
basis of all knowledge. That became clear once again at the analytica
conference, which networks industry and academia every two
years at analytica,” says Prof. Gertrud Morlock from the Justus Liebig
University Giessen, who gave a lecture on a sustainable miniature
laboratory system. “The analytica conference has become one
of the most important scientific conferences worldwide—we heard
that repeatedly in conversations,” says a delighted Susanne Grödl.
Many sessions addressed trends such as the digital and green laboratory,
and were, in some cases, at full capacity due to the excessive
demand. Other lectures dealt with topics such as detecting designer
drugs in forensics, innovative mass spectrometry procedures for the
botanical origin analysis of honey, or special analytical methods for
ancient manuscripts.
analytica 2026 in figures
1,135 exhibitors (2024: 1,066 exhibitors) traveled from 40 countries
and regions, 56 percent of them from abroad. The top ten exhibitor
countries were (in this order): Germany, China, the U.S., Italy, Great
Britain and Northern Ireland, the Netherlands, Switzerland, France,
India, and Spain. There were about 35,000 visitors (2024: 33,386 visitors)
from 115 countries and regions, and the share of international
visitors totaled around 40 percent. After Germany, the top ten visitor
countries were (in this order): Austria, Switzerland, Italy, Great Britain
and Northern Ireland, France, the Netherlands, Turkey, Poland,
Czech Republic and the U.S.
The next analytica will be held with the analytica conference
from April 25 to 28, 2028.
Messe München GmbH
D 81823 München
Regulatory milestone provides planning security for BBIT-based products
Vink Chemicals listed according
to Art. 95 for active ingredient BBIT
Vink Chemicals is officially listed for the active substance
BBIT according to Article 95 of the EU Biocidal Products
Regulation, thereby strategically expanding its portfolio.
With the achievement of this milestone, Vink Chemicals strengthens
its position as a reliable manufacturer of biocides and as a
solution provider that supports its customers with both active substances
and formulated systems.
BBIT is now the seventh active substance listed by Vink Chemicals
under Article 95 of the EU Biocidal Products Regulation. This
confirms and honors the company‘s long-term strategy to commit
to compliance with legal requirements, ensure supply security for its
customers, and continuously expand its portfolio.
Ingo Krull, Technical Sales Manager TB Europe at Vink Chemicals,
comments: „With Vinkocide® BBIT 97, Vink Chemicals completes
its active substance portfolio for water-miscible coolants.
Vinkocide® BBIT 97 was the last missing puzzle piece in our product
range. This means we now offer not only the active substance
BBIT but also a water-soluble formulation with Vinkocide® BB WM,
enabling the use of BBIT in all aqueous metalworking fluids.“
With the listing, Vink Chemicals now has the opportunity to offer a
range of high-performance products based on BBIT. These include
Activink® BBIT 97 (for formulators of biocidal products) as well as
Vinkocide® BBIT 97, which is used as a biocide in liquid concentrates
for metalworking and in the manufacture of silicone sealants.
Furthermore, Vink Chemicals offers ready-to-use formulations
based on BBIT: parmetol® BPX for household, industrial, and institutional
sectors (HI&I), paints & coatings, and coolants, as well as
Vinkocide® BB WM for post-treatment in metalworking fluids.
BBIT products now available
With the listing of Vink Chemicals, customers in Europe now have
a genuine alternative supplier, allowing them to diversify their procurement
risks. Vink Chemicals plans to further develop the market
through competitive conditions and reliable availability. Interested
companies can request samples immediately.
Vink Chemicals
D 21250 Tostedt
What customers now benefit from
Headquarters of Vink Chemicals in Kakenstorf near Hamburg.
(Image: Vink Chemicals)
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The world-leading trade fair sends a strong message with global reach
and innovation power in a challenging market environment
PaintExpo: Worldwide, indispensable
meeting point for industrial
coating technology
Concrete projects, lively conversations, palpable energy – the PaintExpo
presented itself in 2026 at its most dynamic. Intensive discussions
took place in the halls, new contacts were made, and business
was initiated, driven by a high visitor frequency and an international
professional audience. The atmosphere: electrifying. And perhaps
the most surprising aspect: amidst a challenging economic situation,
a clear optimism prevailed, paired with a firm determination to actively
pursue the next steps. „Despite strikes in air traffic and difficult
economic conditions, PaintExpo 2026 was a complete success. It
once again demonstrated that the world’s leading trade fair for industrial
coating technology is the most important impulse generator
and an indispensable platform for the industry,“ explains Markus
Geisenberger, Managing Director of Leipziger Messe.
With 10,200 visitors from 68 countries and 425 exhibitors from
30 countries, it shows that even in its tenth edition, it enjoys very
high acceptance and attracts visitors from all over the world. It is the
must-attend event for new visitors and existing customers. Almost
45 percent of the guests do not participate in any other trade fair. „I
am very satisfied with the great public interest at PaintExpo 2026.
Our booth – as in previous years – was continuously well attended,
and we held many targeted high-level conversations. I am especially
impressed by the high international share of visitors,“ states Michael
Müller, CEO of the WAGNER Group.
PaintExpo has once again expanded its international significance:
the proportion of foreign exhibitors increased from 48 to 52
percent, which also affected the visitor structure. Almost 40 percent
of visitors traveled from abroad, making the fair a global meeting
point for the industry. Industry professionals from 68 countries used
the platform to gather information from companies in 30 different
countries, establish international business contacts, and explore
new markets. This strong international presence promotes crossborder
exchange of know-how and innovations. Thomas Querfurth,
Sales Coordinator for Germany at HangOn, confirms this: „There is
simply no other spot where you can gather in three exhibition halls
and meet all the necessary trades within a few days, exchanging the
latest technology. And this applies to companies from Japan to the
USA.“
Innovations shape the industry: The focus of this year‘s event
was particularly on sustainable, energy-efficient, and digitized coating
processes in the areas of powder coating, wet coating, dip coating,
and electroplating. Automation and the use of artificial intelligence
also defined the trade fair activities and reflected the current
industry requirements, which aim to simplify processes for users,
redefine standards, or increase flexibility. Numerous world and trade
fair premieres demonstrated how companies can make their processes
more economical and environmentally friendly at the same
time. „Personal exchange is especially important to us and cannot
be replaced by digital formats because only in individual conversations
can our technologies, solutions, and services be made visible
and tangible. But the PaintExpo is also relevant as a trend barometer.
Here we see which future application fields can be developed,“ adds
Matthias Haarer, Managing Director at Eisenmann.
Platform for exchange and business initiation: PaintExpo 2026
impressed not only with its comprehensive product and solution
offerings but also as a communication and business platform for decision-makers
and managing directors – after all, two out of three visitors
belong to the top decision-makers in their companies. Intensive
technical discussions, concrete project initiations, and active
exchange between providers and users characterized the trade fair
– a key success factor that has already led to high satisfaction among
exhibitors and visitors in previous events. 89 percent of exhibitors
state that they achieved their goals for participating in PaintExpo.
„PaintExpo simply manages to bring the entire industry to Karlsruhe
and offers a comprehensive showcase of surface technology.
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For Krautzberger, PaintExpo is the most important trade fair there
is,“ explains Thomas Weidmann, Managing Director of Krautzberger
GmbH.
Focus on Nachwuchsförderung (young talent promotion): On
the final day of the fair, PaintExpo also emphasized the promotion
of young talents with its Career Day. Students and graduates received
targeted insights into industrial coating technology and could
directly contact companies. A compact program of lectures, guided
tours, and networking offered practical orientation regarding entry
opportunities and career paths. This strengthens PaintExpo’s role as
a platform for networking professionals and industry.
The focus is already on the next event: The upcoming PaintExpo
will take place from April 25 to 28, 2028, and already attracts interest.
Numerous exhibitors are already using the opportunity of rebooking
during the ongoing fair to secure their preferred spots early.
Leipziger Messe GmbH
D 04356 Leipzig
Redipor® Legionella agar plate range - specifically designed to support the detection
and enumeration of Legionella in water samples
New Legionella testing selective
agar plates launched by AnalytiChem
AnalytiChem’s new Redipor Legionella agar plates,
specifically designed to detect and count Legionella bacteria
in water samples.
AnalytiChem, manufacturer of specialized laboratory equipment,
reagents and consumables, has launched a new addition to its highquality
Redipor® microbiological prepared media portfolio. The new
Redipor Legionella Agar Plate range offers a suite of ready-to-use,
selective culture media options. These are formulated to support
ISO 11731-compliant Legionella culture workflows, enabling enumeration
of Legionnaires’ Disease-causing Legionella spp. bacteria as
colony-forming units (CFU) for regulatory reporting.
AnalytiChem’s new Redipor Legionella media range covers the
full culture pathway required for ISO-aligned testing, ensuring reliable
recovery, quality control, and compliance with international
standards. This makes it ideal for use in laboratories and organizations
responsible for water safety and regulatory compliance, including
environmental, public-health and industrial monitoring laboratories,
as well as water utilities.
Redipor Legionella media delivers a comprehensive range of ISO
11731–aligned culture media, designed for parallel plating on non-selective
and selective media, as required by ISO 11731 to maximize
recovery across diverse environmental sample types. Plate options
include BCYE (Buffered Charcoal Yeast Extract), GVPC (Glycine
Vancomycin Polymyxin Cycloheximide) and MWY (Modified Wadowsky-Yee)
agar variants with growth factors and selective agents,
and a cysteine-free option for comparative studies.
Each Redipor medium in the new range serves a distinct role
within the Legionella culture workflow: non-selective recovery
(BCYE), selective isolation (GVPC, MWY), and confirmation via
cysteine dependency. AnalytiChem experts can advise on the right
combination by application - from testing clinical respiratory specimens
(e.g. BAL, sputum) to differing environmental water or heavily
contaminated environmental samples, such as biofilms and cooling
tower sludge.
“Culture remains the internationally accepted reference method
for the detection, enumeration, and confirmation of Legionella
in water systems, forming the basis of regulatory compliance and
outbreak investigation,” said Nico van Stallen, Segment Director
Life Science & Lab Essentials, AnalytiChem. “Our new suite of ready‐to‐use
Redipor Legionella agar plates are designed to make this
workflow simple, consistent, and aligned with ISO 11731. This is the
benchmark international reference method for Legionella detection,
supporting official investigations and reporting.”
AnalytiChem’s Redipor ready-to-use culture media range not
only supports critical applications in Water testing, but also Pharmaceutical
quality control, Food & Beverage, and Healthcare sectors.
AnalytiChem Holding GmbH
D 65760 Eschborn
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Interpack 2026: Stäubli presents a comprehensive robot
portfolio for hygiene-sensitive applications
Roboter für Food- und
Pharma-Packaging
At Interpack, Stäubli emphasizes its expertise in Food and
Pharma Packaging with groundbreaking innovations at
booth C38 in Hall 15. The manufacturer has expanded its
portfolio of hygienic four- and six-axis robots with a mobile
pharmaceutical robot capable of operating even under sterile
conditions – a true world first.
TX2-160 HE - Both the SCARAs
of the TS2 series and the TX2
six-axis robots prove themselves
in the wash-down version (HE)
configuration with food-grade oil
(H1) in all possible applications
in food manufacturing.
(Copyright: Stäubli Tec-Systems
GmbH Robotics)
With the Accesspharma program, which
focuses on environments of cleanroom class C,
Stäubli completes the circle with fast, reliable
automation solutions for non-aseptic areas.
(Copyright: Stäubli Tec-Systems GmbH Robotics)
In sensitive industries such as food, pharmaceuticals, and medical
technology, special regulations, specific standards, and strict hygiene
requirements apply. These entry prerequisites naturally create
a barrier to robot deployment. Therefore, standard robots are at best
found in secondary packaging areas.
For all other tasks, such as packaging open foods or filling liquids
into vials, robots that meet the strictest hygiene standards, including
sterilization, are required. Additionally, process safety, dynamics,
and precision are among the desired qualities.
With numerous model variants of four- and six-axis robots,
Stäubli can precisely meet these industry-specific requirements.
Now, the provider has further enhanced its unique robot portfolio
with two additional innovations. „At Interpack, we will present,
alongside two demo applications, the TX2-60L Stericlean+ in Hollow
Wrist design as well as the Sterimove, the world‘s first mobile
robot capable of working under sterile conditions. This is a milestone
for the pharmaceutical industry,“ says Peter Pühringer, Managing
Director of Stäubli Robotics.
Sterimove – a globally unique concept
Indeed, Sterimove is more than just an innovation. The mobile robot
makes a significant contribution to safer, more productive, and
more reliable pharmaceutical manufacturing. The device sets new
standards for mobile robotics in Class A/B/C/D environments. Sterimove
minimizes contamination risks from manual interventions,
increases productivity, and ensures safety and reliability in the most
sensitive environments. Thanks to its modularity, easy cleaning, and
contamination-free design, it is the ultimate solution for pharmaceutical
manufacturers seeking safety and operational excellence.
Special versions: From HE and H1 to Stericlean and Stericlean+
Both the SCARAs of the TS2 series and the TX2 six-axis robots perform
reliably in the wash-down configuration (HE) with food-grade
oil (H1) across all possible applications in food production. When it
comes to meeting aseptic conditions, these four- and six-axis robots
are also available in the Stericlean version. For direct use in isolators
within high-sterility pharmaceutical environments of GMP Class A,
Stäubli offers the suitable robot with the Stericlean+ variant.
For the first time at Interpack, Stäubli will present the TX2-60L
in Stericlean+ version with Hollow Wrist. „With these robots, the
engineers have pushed the hygienic design to the limit with a fully
enclosed structure from the base to the flange at the tip. The model
with hollow wrist offers unparalleled cleanability and improves
decontamination processes compared to the standard model,“ emphasizes
Pühringer. The cleaning processes are simplified, and the
robot‘s design additionally prevents particles from adhering to the
coating. The Stericlean+ option with Hollow Wrist for the TX2-60
and TX2-60L models is now available for order.
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Practical demo applications
Fully automatic filling and packaging of radionuclides.
(Copyright: C-RayTherapeutics Group)
At Interpack, Stäubli will showcase the performance of its robots
through two application examples in the Food and Pharma sectors.
In an AI-optimized, robot-assisted food application, a TS2-80 SCA-
RA in HE and H1 versions demonstrates high dynamics in handling
unpackaged foods. A special feature: the SCARA is equipped with
a newly designed bellows made from material properties compliant
with FDA guidelines. This makes the robot suitable for direct contact
with food.
A second cell demonstrates the advantages of the recently introduced
Accesspharma series in the secondary packaging of pharmaceuticals.
With the Accesspharma program, focused on cleanroom
environment Class C, Stäubli completes the circle with fast, reliable
automation solutions for non-aseptic areas. This allows users to
avoid the significantly higher investment in more complex model
variants.
Stäubli Tec-Systems GmbH Robotics
D 95448 Bayreuth
Technical surface coatings for
3D-printed plastic parts
In mass production, 3D-printed parts are being used to an increasing
extent – not only for small batches and prototypes. Therefore, it
is of great importance that the surface quality of the parts is optimized
in every respect. With our processes and procedures, we bring
3D-printed components and housings to the level of commercial
parts in terms of appearance and function.
On one hand, regarding the visual appearance, which is especially
important for visible components. On the other hand, in many
cases, the technical properties of the surface of the parts are also significant.
Here, our diverse methods and variations of surface coating
are available to meet various requirements.
The surface technology that WÖHR covers includes
the following applications:
– Increasing chemical robustness
– Enhancing UV resistance
– High-ohmic ESD protection
– Low-ohmic EMC protection
Structurally, a coating can also offer advantages; depending on the
choice of coating, different surface textures from fine to coarse can
be applied to the workpieces.
Does your 3D part have the wrong color because the filament for
the 3D printer is not available in the desired shade? Our coating systems
allow for a free choice of color to match other components of a
device – even metallic-looking surfaces can be realized. We can also
vary the gloss level of the surface.
Defects in the surface, such as small holes or fine seam lines, can
be invisibly covered with a coating. With our expertise, we adjust the
surface of the coating so that cracks, holes, and seams are no longer
visible.
The advantage of all our coating technologies for our customers: they
receive ready-to-sell parts and components that are suitable even for
demanding users – including the renowned excellent quality of Richard
Wöhr GmbH.
Richard Wöhr GmbH
D 75339 Höfen/Enz
Oberflächenlackierung 3D-gedruckte Kunststoffteile – Vergleichsbild
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34th Conference „Industrial Component Cleaning“, June 25 and 26, 2026
Ensure component cleanliness in
a process-safe and efficient manner
Changed requirements for the quality, cost-efficiency, and sustainability of components
demand adapted manufacturing technologies and processes – including
in component cleaning. As a leading knowledge platform in the German-speaking
region, the „Industrial Component Cleaning“ conference of FiT provides
relevant know-how, informs about trends and new developments in cleaning
technology. The event program with an integrated exhibition on June 25 and 26,
2026, at the Neckar Forum Esslingen also includes the presentation of the 5th
FIT2clean Award.
Increasingly rapid transformation processes
in industry pose challenges for manufacturing
companies. For example, producing
high-quality components and system parts,
including for sensor and analysis systems,
aerospace, semiconductors, optics, mobility,
medical and pharmaceutical technology,
security technology, defense, coating and
finishing technology, as well as energy technology,
requires optimized and new solutions
even in component cleaning. The processes
must ensure that defined, sometimes
extremely strict cleanliness specifications
are not only stable and cost-efficient but
also carried out in an energy- and resourcesaving
manner.
The 34th „Industrial Component Cleaning“
conference of the Professional Association
for Industrial Part Cleaning (FiT)
presents know-how, new process engineering
solutions and products, innovative
methods for process control, as well as bestpractice
applications. An integrated exhibition
and the presentation of the „FiT2clean
Award“ innovation prize complement the
program of this event, established as a leading
knowledge platform for component
cleaning. It will be held by fairXperts on June
25 and 26, 2026, at the Neckar Forum Esslingen.
Future-oriented cleaning
processes – what matters
The focus of the versatile two-day program
includes the areas of process chain for component
cleaning, media quality – process
water treatment, innovations, measure-
ment, testing, and control, as well as practical
examples. It offers numerous impulses
and shows strategies for adapting and optimizing
cleaning processes. Under the title
„From Sand in the Gears to Contamination-
Free,“ the importance of purity throughout
the entire process chain is examined, along
with general standards, guidelines, and
practical requirements. A presentation will
illustrate the conceptual and technological
challenges in designing high-purity cleaning
applications using a case study from medical
technology, where the cleaning system is
understood as a quality gate before the cleanroom.
The factors to consider when coordinating
forming processes, component
cleaning, and corrosion protection in battery
cell manufacturing are also discussed.
The agenda also features the introduction
of a world novelty for energy-efficient and
environmentally friendly laser cleaning of
mass-produced items such as screws, nuts,
or clips. Under the motto „Innovation Butane
Cleaning,“ participants will receive an
update on the latest developments of a new
cleaning process. Other topics include new
high-performance filters for component
cleaning and the efficiency advantages of
treating used rinse water through vacuum
distillation. Additionally, the conference will
inform about ways to increase cleaning efficiency
and recycling capability of process
water during vibratory finishing through
synergistic cleaning and flocculation systems,
as well as cost and resource savings in
Defines, partially extremely strict cleanliness specifications that are
both stable and cost-efficient as well as energy- and resource-saving,
for which the conference offers knowledge, innovations, and solutions.
(Image source: fairXperts GmbH & Co. KG)
The accompanying exhibition provides direct information
about new products, developments, and networking.
(Image source: fairXperts GmbH & Co. KG)
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The event in brief:
34th „Industrial Component Cleaning“ Conference
Date: June 25 and 26, 2026
Location: Neckar Forum Esslingen, Hauffstraße, 73728 Esslingen
Information and registration: www.industrielle-reinigung.de, fairXperts GmbH & Co. KG,
Nicolas Herdin, nicolas.herdin@fairxperts.de
component cleaning through sensor-controlled
bath changes. New developments for
bath monitoring, such as a solution for mobile
measurement of ultrasonic power and
cleanliness control regarding particulate
and film cleanliness, will also be presented.
The benefits resulting from the interplay of
cleaning technology and new measurement
solutions along the process chain are illustrated
with practical examples. Just as the
consistent recording, evaluation, and interpretation
of process and cleanliness data
can enhance cleaning performance.
Furthermore, the decisive influence of
intelligent parts handling on cost efficiency
is highlighted. The question of what advantages
inline laser cleaning of aluminum diecast
electronic housings offers as an alternative
to decapping is answered by a practical
contribution.
Presentation of the FiT2clean
Innovation Award
As part of the conference, the €10,000 FiT-
2clean Award will also be presented. The innovation
prize will be awarded for the fifth
time on June 25. Prior to that, the three finalists
will present their submitted solutions to
the conference participants.
Accompanying exhibition
– networking at its best
An accompanying exhibition rounds off the
demanding lecture program. Participants
Fachverband industrielle Teilereinigung (FiT) e.v.
Geschäftsstelle
Hauptstraße 7
D 72639 Neuffen
Telefon: +49 7025 84340 Telefax: +49 7025 843420
eMail: info@fit-online.org
Internet: http://www.fit-online.org
Reingehört special, live from the lounges Karlsruhe 2026, the first episode of the year
with Dr. Jochen Kolb, Managing Director of BioChem Labor für biologische
und chemische Analytik GmbH, Karlsruhe
Reingehört - the podcast of the cleanroom
and process engineering industry
From the comprehensive analysis and
consulting services of BioChem, including
what the horseshoe crab has to do with bacterial
analysis, to home water filters – in this
episode, everything revolves around water.
What qualities does water have in pharmaceutical
production?
The podcast discusses, among other
things, the monographs of Ph. Eur., USP, and
JP and their differences. For example, Ph.
Eur. has recently included the rFC test in the
endotoxin LAL test monograph. This test is
more sustainable than the LAL and does not
rely on animal products.
BioChem also talks about problems in
the production and supply of water in pharmaceutical
manufacturing (e.g., biofilm).
will have the opportunity to learn about new
products and developments in industrial
cleaning technology and to exchange experiences
directly with experts.
The conference is aimed at specialists
and managers, engineers, and technicians
from development and design, technology,
process engineering, work preparation,
manufacturing, production planning, and
quality management from various industries.
The complete program of the 34th „Industrial
Component Cleaning“ conference,
further information, and registration forms
are available at www.industrielle-reinigung.de.
https://open.spotify.com/episode/3kJIw2U-
RY4N4bPD7sxAvIo?nd=1&dlsi=02e2f133499c4675
BioChem Labor für biologische und chemische Analytik
GmbH
Daimlerstr. 5b
D 76185 Karlsruhe
Telefon: +49 721 9737-0
eMail: biochem@biochem.de
Internet: http://www.biochem.de/
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With SynTiso, developed together with two major pharmaceutical companies,
Syntegon offers the solution for increasingly strict regulations
aimed at eliminating contamination risks in injectable medicines.
interpack 2026: „re:imagine Your Factory
of the Future“ – with the strategic
lifecycle partner Syntegon
– The „Factory of the Future“ of pharmaceutical, biotech,
and food companies must address urgent industry challenges
– Automation, robotics, digitalization, and AI enable users
to focus on value-adding tasks
– Syntegon‘s contribution to „re:imagine Your Factory of the Future“:
neXt, SVX, SynTiso – supported by lifecycle services
At interpack 2026, Syntegon will reimagine the „Factory of the Future“
together with its customers (re:imagining) and present solutions
to their most pressing challenges. With highly innovative solutions,
the company will demonstrate at stand A31–B31 in Hall 6 how
processes in the pharmaceutical, biotech, and food industries can be
elevated to the next level of efficiency, flexibility, and sustainability.
Challenges as Drivers
for Innovation and Growth
The industry is undergoing a groundbreaking transformation: Due
to increasing cost pressures, growing flexibility requirements, and
stricter regulations, companies must rethink the „Factory of the
Future.“ Syntegon addresses these challenges through innovations
developed jointly with customers. The vision: a factory that regulates
itself and adapts to all challenges, overseen by an AI-supported
human control center. At interpack 2026, Syntegon will present the
building blocks that enable customers to rethink their „Factory of the
Future“ – with processes that are smoother, smarter, contactless, and
ultimately more efficient.
„At interpack, we demonstrate the strength of our COCREA-
TE and COSUCCEED concepts. Breakthrough innovations developed
together with customers lead to greater business success.
Our highlights neXt and SVX set new standards in the food sector.
In pharmaceutical production, SynTiso sets a new standard as the
first of its kind: a glove-free high-speed line for filling liquid medicines.
Syntegon‘s promise as a strategic lifecycle partner combines
industry leadership with top-tier lifecycle services as the
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The new neXt system solution from Syntegon addresses the industry‘s
challenges by offering seamless operation, smart performance, and
contactless control.
ultimate enabler for our customers‘ growth,“ says Torsten Türling,
CEO of Syntegon.
neXt: The „Factory of the Future“ is smooth, smart,
and contactless
The food industry is developing rapidly: consumer and retailer demands
change overnight, requiring maximum flexibility. Workforce
shortages and rising costs, along with regulations demanding more
sustainable packaging materials, are pressing issues. Syntegon‘s
new system solution neXt addresses these challenges with seamless
operation, smarter performance, and contactless control. The neXt
automation allows users to focus on value-adding activities.
Smooth processes increase efficiency and minimize downtime.
Real-time data drive fact-based decisions and optimized OEE. Contactless
operation and intuitive user interfaces lead to faster changeovers,
reduced training efforts, and higher flexibility across the entire
product portfolio. Looking ahead to future requirements, neXt gives
food manufacturers a competitive advantage in a dynamic market.
SVX: High speed, quick changeovers,
low material consumption
The highly innovative vertical packaging platform SVX sets new
standards in meeting current and future customer requirements. Its
impressive speed of 300 bags per minute enables the lowest cost per
bag. Switching between different bag formats is simple, quick, and
ensures maximum availability and flexibility. Patented technology
reduces packaging material consumption by 50 percent. The compact
footprint of the SVX significantly increases productivity per
square meter without requiring additional production space, thereby
supporting business growth.
SynTiso: Redefining liquid
pharmaceutical production
Pharmaceutical and biotech are growth industries. Most new biologics
are delivered as injectable preparations. Stricter regulations
aim to eliminate contamination risks in injectable drugs. Syntegon
offers the solution with SynTiso: developed jointly with two major
The highly innovative vertical packaging platform SVX sets new
standards in solving today‘s and future customer requirements.
pharmaceutical companies, SynTiso eliminates the need for human
intervention through glove-free isolator technology and fully robotic
operation, including contactless transport systems. The advantages:
compliance with the highest regulatory standards, 50 percent faster
changeovers, and higher batch outputs. SynTiso is ready to revolutionize
the future of liquid drug filling.
“re:imagining Your Factory of the Future”
with Lifecycle Services
Syntegon is the strategic lifecycle partner for its customers. Its comprehensive
application expertise supports companies in the pharmaceutical,
biotech, and food industries from the initial idea stage
for their „Factory of the Future.“ Engineering solutions tailored to
the specific business needs create the best return on investment.
Flawless project execution from start to production enables faster
market entry. Qualified service engineers on-site ensure reliable
performance and high availability. Continuous line upgrades based
on AI-supported data analysis make every investment future-proof.
Syntegon‘s lifecycle services turn the equipment of any „Factory of
the Future“ into a valuable and reliable business asset.
Syntegon Technology GmbH
Blaufelder Straße 45
D 74654 Crailsheim
Telefon: +49 7951 4020
eMail: packaging-ph@syntegon.com
Internet: http://www.syntegon.com
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Arburg Technology Days 2026
The leading information platform
for all plastics processors
– A success: The industry’s largest in-house event worldwide, attracting around 3,750 visitors
– arburgSOLUTIONworld: Practical solutions, high performance and 40 machine exhibits
– Highlight: New electric Allrounder Trend machines receive an enormous response
Around 3,750 visitors from 44 countries attended the Arburg Technology Days from 11 to 13 March 2026, dedicated entirely
to arburgSOLUTIONworld. This industry highlight once again impressed with its tried-and-tested concept of opening the
doors of Arburg’s central headquarters in Lossburg to its German and international customers. With more than 40 machine
exhibits and a wide range of practical applications, innovative processes, smart automation, as well as digital services,
software and after-sales offerings, Arburg demonstrated its capabilities in every respect – from standard to high-end. The
company presented itself across the entire value chain as an innovative solution provider and as a competent and reliable
partner.
The guests were thoroughly delighted to learn more about the present
and future of injection moulding – from the new electric Allrounders
Trend through special exhibition areas dedicated to medical
technology, sustainability, automation and turnkey solutions, to
specialist presentations, a comprehensive service area and insights
into the state-of-the-art assembly line for the Trend machines. There
was also ample opportunity for networking and for one-on-one
discussions with the experts from Arburg and its partners.
Once again, unique for the entire industry
“Presenting the wide range of solutions – the unique blend of technology,
processes and services – all in one place makes the Arburg
Technology Days the ‘home of injection moulding’, a showcase for
plastics processing and a magnet for customers from all over the
world”, summarised Juliane Hehl, Managing Partner Global Marketing
and Business Development at Arburg. “Nowhere else is such
a wealth of information concentrated in such a customer-focused
way. We see ourselves as a highly reliable partner who cultivates
the best possible business relationships over the long term. With us,
everyone finds exactly the right answers to their individual injection
moulding questions of today and tomorrow. We had many fruitful discussions
and received substantive enquiries about our machines,
services and solutions”.
Dr Christoph Schumacher, Vice President Global Marketing,
adds: “These Technology Days are a fixture in the trade fair calendars
of our customers and prospective clients. The high level of
commitment and customer focus shown by each and every one of
us leaves an extremely positive overall impression. This makes a visit
to the Technology Days an experience within and alongside the Arburg
family.”
Hands-on experience: Allrounder Trend highlight
Ein Highlight unter den rund 40 Maschinen-Exponaten der
Arburg Technologie-Tage 2026 waren die elektrischen Allrounder
Trend – der neue Standard im Spritzgießen. (Foto: ARBURG)
Five exhibits of the electric Allrounder Trend demonstrated how rapid
set-up and simple operation enable the efficient production of
plastic parts. The new standard machines are available worldwide.
At the market launch in spring 2026, four machine sizes with clamping
forces ranging from 500 to 2,000 kN will be available. The following
exhibits could be experienced live:
– A typical application for technical injection moulding was the
production of free-falling, angled insulators for automotive wiring
harnesses on an electric Allrounder 1000 e Trend.
– An automated Allrounder 1000 e Trend attracted a great deal of
attention as it produced the “Donut-ella” – a practical USB cable
winder – from PA material recycled from abandoned fishing nets.
The gadget was the winner of the Italian “Pleiades” design competition
of the IUAV University of Venice. Arburg supports this
competition with machine technology; other partners include
Uniform (mould) and Ewikon (hot runner).
– An electric Allrounder 500 e Trend produced reusable coffee
cups made from coffee grounds. The bio-based compound and
tool for this came from the Danish start-up Grounded.
– The efficient production of 9,200 LSR closures per hour was
demonstrated on a production cell centred around an Allrounder
1800 e Trend with a 64-cavity tool from ACH Solution and a linear
Multilift Select 16.
– The new Gestica lite control system for the Allrounder Trend also
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attracted enormous interest from visitors. It is simple and intuitive
to use and features a clear, centralised dashboard that is easy to
understand. This makes the machine much easier to oerate, even
for non-specialists.
Automation and turnkey solutions take centre stage
Skills shortages and labour costs are increasingly pointing a spotlight
at customised automation and turnkey projects into focus. Arburg
sees itself in every respect as a “problem solver”, finding turnkey
solutions that keep unit costs to a minimum without compromising
maximum quality in any way. The turnkey experts offer expertise tailored
to the specific case of application and support the customers
throughout the entire value chain, from the initial idea to the finished
product. Several customer projects and Arburg exhibits demonstrated
succinctly, how ingenious ideas and efficient automation can
be put into practice.
To showcase this, e. g. a turnkey system centred around a vertical
Allrounder 475 V produced covers for radio keys as an example.
Here, overmoulding with PC/ABS recycled material combined
with in-mould decoration (IMD) creates a high-quality surface. Part
handling and re-working are carried out by a Kuka six-axis robot integrated
into the Gestica control system.
– One benchmark project is the digitally interlinked turnkey system
for injector pens, the “NextGen Medical Solution”, centred
around an Allrounder 570 A electric machine in cleanroom version.
This production cell was realised through the collaboration
of Arburg (machine technology), Hack Formenbau (mould technology),
Hack Digital Solutions (mould monitoring), HB-Therm
(temperature control units) and a renowned OEM. It impresses
with a holistically optimised, cost-effective, compact configuration
characterised by high availability, productivity, part quality
and energy-efficiency.
– An Allrounder 370 A electric injection moulding machine demonstrated
how medical products can be manufactured in an
ISO Class 7 clean room under the most stringent of hygiene standards.
The dual-cavity pilot mould from partner Fostag can be
scaled up to a large number of mould cavities once the part design
has been finalised.
– A cost-effective investment is to connect a clean room-rated
machine to the clean room via an extended tunnel conveyor belt.
This was demonstrated on an electric Allrounder 520 A. Using a
96-cavity tool from partner Kebo, around 60,000 needle caps for
insulin pens made from PP (Borealis) were produced per hour.
These were then fed into the clean room on an enclosed conveyor
belt.
– Using a demo part for microfluidics, a hydraulic Allrounder 520 S
demonstrated, a simple, reliable and cost-effective way of manufacturing
medical products from PVC, known as a difficult material
to process.
– Is there a reliable process for achieving shot weights of just 0.016
grams? This is precisely what a production cell based around
an electric Allrounder 270 A set out to demonstrate. The machine
was equipped with a size 5 micro injection module and
an 8-millimetre injection screw and it showcased the sprueless
production of four micro-filters, each weighing 0.004 grams and
featuring complex geometries.
High levels of public interest across the board
570A NextGen Medical Solution (Foto: ARBURG)
Focus on Medical: Diverse clean room solutions
Arburg had set up a dedicated “Medical Corner” for the expanding
medical sector. This showcased some pioneering exhibits from the
field of medical technology – developed by Arburg and renowned
partners: stand-alone solutions, a production cell docked to a clean
room, and production directly within that clean room – an appropriate
concept to meet every requirement.
Other key areas of the Arburg program also proved very popular
with visitors. Considerable interest was shown in digital services
and software across the entire value chain. Many of these solutions
enable customers to minimise their operating costs and thus save
money. Here, Arburg provides support with its combined expertise
in digitalisation, smart manufacturing and artificial intelligence. The
Gestica lite control system, Arburg’s own MES (ALS) and the arburgXworld
customer portal were presented. In addition, the added
value of innovative digital pilots and assistants was demonstrated on
Allrounder exhibits.
In the arburgGREENworld exhibition area, the company demonstrated
what it has to offer in terms of processing recycled materials
and alternative plastics, as well as the activities contributing
to resource conservation and the implementation of a functioning
circular economy.
The wide range of Application Technology services was also
showcased, including on-site consultancy, fault analysis and process
optimisation. In the service area, the range of services covering the
entire machine lifecycle was on display. Here too, the focus was on
‘ease of use’. These machines are easy to operate and maintain. This
enables even relatively inexperienced operators to manufacture products
of the highest quality. The maintenance of the new Allrounder
Trend, predictive maintenance, comprehensive after-sales support
and Ready2Go used machines, as well as modern training methods,
were demonstrated.
The technical presentations on all three Technology Days were
complemented by interesting expert talks. These offered practical
insights – from reliable injection moulding and the path to the
Smart Factory right through to the latest Allrounder Trend machines.
And last but not least, the factory tours were also very well received.
Among other things, interested visitors were able to find
out in detail about the new Allrounder Trend production concept
and gain interesting insights into the highly automated production
at Arburg.
ARBURG GmbH + Co KG
D 72290 Loßburg
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The pharmaceutical and valve
industry – a marriage
for life
In order to eliminate the
risks associated with manual
handling, SISTO Armaturen S.A.
developed an automatic media
panel as a compact, flow-optimised
multi-way block diaphragm valve.
(Source: KSB / SISTO)
Everything communicates with everything else – in the
pharmaceutical industry, this type of production process
has long been more than just a vision for the future. Already,
artificial intelligence and the digital transformation are
streamlining the first pharmaceutical plants. Good news for
an industry which in many countries is one of the important
pillars of their economy.
The pharmaceutical industry is accelerating the digital transformation
of its laboratories in order to make them more efficient and
sustainable. “Large pharmaceutical companies are planning to nearly
double their investments in laboratory transformation by 2025
– from 4 percent today to as much as 7 percent of their turnover,” the
Capgemini Research Institute (CRI) reports. Almost 75 percent of
drug companies have already started modernising their laboratories.
“Cost pressure and international competition are increasing,”
explains the Baelz company, a provider of valves, actuators and sensors
and more. In order to remain competitive in a challenging environment,
the focus is therefore increasingly on digitisation. “It is
indispensable both for the use of valves and the management of our
plant park,” reports Baelz. Everything communicates with everything
else.
Sanofi also continuously invests in its facilities. The goal is, among
other things, to strengthen Europe‘s supply security in the
pharmaceutical sector. (Photo: Sanofi)
Automation and digitisation as a key
Automation and digitisation are progressing – a development also
observed by Baelz. For example, a pharmaceutical company invested
around 275 million Euros into a highly automated model factory for
the treatment of cancer and cardiovascular conditions. “Thanks to
With FLOWave, Bürkert has brought a hygienic, material-saving and yet
very accurate flow sensor to the market. The focus was on conserving
resources. (Photo: Bürkert Fluid Control Systems)
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its modular design, you can quickly expand or convert production,”
says Baelz.
A Baelz pure steam generator station was designed specifically
in order to provide live steam for the production of drugs in their new
production building. “Sophisticated control and safety functions as
well as integrated automatic desalination and sludge removal ensure
a smooth and economical operation,” explains Baelz.
Optimising energy needs
Increased energy prices are proving a challenge for the pharmaceutical
industry. The sector is therefore taking action and installing
new plant or optimising existing systems with regard to their energy
requirements. Against this background, Bürkert has developed products
that are not just more energy-efficient to manufacture, but
also reduce energy consumption in subsequent use. Therefore, Bürkert
is continuously investing into the development of components.
In addition, the company is also trying to think of system solutions
that offer increased added value to their customers. An example of
this is their FLOWave flow sensor: “The use of an innovative physical
sensor principle has enabled us to launch a hygienic, material-saving
and very accurate flow sensor.”
Sterile, aseptic and hygienic processes
A variety of pharmaceutical processes require safety valves in a variety
of materials and sizes. “Especially in the core processes for the
end product, there is a need for special valves that offer easy process
integration with the option of cleaning (CIP) or sterilisation (SIP),”
explains the valve manufacturer LESER. “Safety valves for these applications
must avoid external contamination.”
With their Clean Service series, LESER has developed safety
valves “that meet all the requirements of the pharmaceutical industry”.
Its small dead space and gap-free interior construction
allow for “a high degree of cleanliness”. During the cleaning process,
valves can be opened automatically using the existing pneumatic
lift.
For use in sterile, aseptic and hygienic processes, valves must
meet high requirements. Since product and process safety is a top
priority in these applications, the GEA industry group has equipped
its aseptic valves with a hermetic sealing element to prevent
microorganisms entering a sterile process. Numerous valve types
are required. The spectrum ranges from shut-off, double-seat and
tank valves to an extensive portfolio of special valves.
Fast, safe and cost-effective
Faced with a strong and changing pharmaceutical industry, valves
are in great demand. SISTO Armaturen S.A. for example, which is
part of the KSB Group, has developed an automated media panel solution
for the production of immunosuppressants for a French pharmaceutical
company. In order to eliminate the risks associated with
manual handling, SISTO developed the media panel as a compact,
flow-optimised multi-way block diaphragm valve. Equipped with
pneumatic drives and electronic feedback units, it automates and
streamlines production processes. “This allows them not just to be
run faster and more safely, but also more cost-efficiently,” emphasises
SISTO.
Investments into modern pharmaceutical plant
The willingness of the pharmaceutical sector to adapt to industry
growth involving increasing requirements by means of investments
is great. There are numerous projects to demonstrate this. With an
investment volume of almost 300 million Euros, Pfizer has expanded
its existing plant into one of the world‘s most modern production facilities
for the pharmaceutical industry in accordance with Industry
4.0 standards. In their “HighCon” factory, drugs for the treatment of
diseases such as cancer, cardiovascular conditions and Covid-19 are
efficiently manufactured for the global market.
The HighCon system facilitates a highly automated and at the
same time sustainable production process. Pfizer: “All machines and
processes are intelligently networked using information and communication
technologies, enabling the Freiburg Pfizer plant to produce
in a faster, more flexible and resource-efficient way.”
Strengthening supply security
In the construction of new facilities, Sanofi also
emphasizes a high degree of automation and the highest
sustainability standards. (Photo: Sanofi)
In Frankfurt, Sanofi is building a state-of-the-art insulin production
facility around 36,000 square meters in size. “The aim is to secure
the long-term supply of vital insulin and to strengthen the European
security of supply,” explains the company. The investment amounts
to about 1.3 billion Euros by 2029. This system will also be largely
automated and is designed to meet the highest sustainability standards.
Merck is also investing sustainably. The company is expanding
its ADC production capacity in St. Louis, USA, by investing 70 million
Euros. Capacities for the production of ADCs (antibody-drug
conjugates) for cancer patients will be tripled, and laboratories modernised.
Such investments by the pharmaceutical industry are also
investments into people’s recovery. The valve industry is part of a
marriage for life, sometimes also helping to save lives in their role as
a supplier.
Trends and highlights from the valves industry can be experienced
at VALVE WORLD EXPO from 1 to 3 December 2026 in Düsseldorf.
Current industry and product information can be found on the
internet portal at www.valveworldexpo.com.
Messe Düsseldorf GmbH
D 40001 Düsseldorf
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Hose and injection molding solutions from Germany | Medical technology expertise
Masterflex Group Medical Solutions
at MedtecLIVE 2026 in Stuttgart
Masterflex Group Medical Solutions: Medical Tubing,
Injection Molding & Assemblies from a Single Source
Plastics are indispensable in medical technology: they enable safe,
reliable, and cost-effective solutions for applications with high requirements
for functionality, documentation, and quality. As Masterflex
Group Medical Solutions, Novoplast Tubing Technology from
Halberstadt and Fleima-Plastic from Wald-Michelbach develop and
manufacture high-quality medical tubing, connectors, injectionmolded
parts/form parts, as well as customer-specific assemblies for
demanding medical applications.
Medical Technology: Development Partner,
Manufacturer, Supplier, and Exhibitor
„Our precise plastic components are used in infusion, dialysis, endoscopy,
enteral nutrition, and also in hearing aids, among others.
A particular advantage for development and purchasing teams: For
many years, we have successfully combined extrusion and injection
molding in complex medical technology projects – thus creating innovative,
economical system solutions from a single source,“ says
Martin Oye, Managing Director of Medical Technology at Novoplast
Tubing Technology and Fleima-Plastic.
Exhibitor at Medical Technology at MedtecLIVE with T4M 2026
Novoplast Tubing Technology will showcase at MedtecLIVE with
T4M 2026 (May 5-7, Hall 3/303) how demanding medical plastic
components can be reliably brought into series production, from
marking to validation. One focus is laser marking under cleanroom
conditions (ISO 14644): this creates durable, wipe- and abrasion-resistant
markings on tubing and plastic components, such as graduations
or serial and batch numbers. Additionally, the Medtec brands of
the Masterflex Group support tool and production relocation in injection
molding – with clear project structure and a consistent focus
on process stability. Complementarily, Novoplast offers validation of
plastic components and downstream processes: compliant, fast, and
audit-proof, as an important contribution to reliable market release.
The German Medtec brands position themselves as trusted
development partners for medical plastic components and support
projects from concept to series production – including project
management, feasibility analyses, and assistance with quality and
regulatory issues.
Free Tickets for MedTec 2026 Medical Technology Trade Fair
Novoplast Tubing Technology invites you to a personal exchange at
MedtecLIVE with T4M 2026 in Stuttgart: whether you want to clearly
mark a product, need a customer-specific injection molding component
or a secure tubing solution, or seek support with validation
and process setup, you can discuss these topics directly with the experts
on site. Hall 3 | Stand 303 (May 5–7, 2026).
Masterflex Group
D 45891 Gelsenkirchen
(Copyright: Masterflex SE)
Medical technology - Fleima-Plastic & Novoplast Schlauchtechnik, booth
3056 at MD&M West 2025, Anaheim. (Copyright: Masterflex SE)
Trade fair stand POV (Copyright: Masterflex SE)
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The new PowerPulse CNp with
ultrasound requires only 2.2 m² of floor
space and features full-current filtration and
separate infrared vacuum drying. (Photo: LPW)
New from LPW: PowerPulse CNp system with ultrasound
High Performance
in the Production
Environment
Requires minimal floor space and offers maximum High Purity technology:
the new PowerPulse CNp with ultrasound from LPW Reinigungssysteme
GmbH. The compact, semi-automatic system was
designed for demanding industrial applications in production environments
and offers high performance, especially at low throughput
rates, high-quality auxiliary processes, and in sensitive manufacturing
areas.
The PowerPulse CNp is designed as a multi-stage system and
functions as a complete unit with manual batch handling. It combines
impulse vacuum through cyclic nucleation (CNp) and ultrasound.
Both methods can be used simultaneously or selectively
depending on the cleaning task. Additionally, the system features
an integrated full-stream filtration that ensures stable process conditions
and supports near-production, low-maintenance operation.
Another essential component is the integrated vacuum infrared drying
as a standalone process stage. It is an integral part of the concept
and enables efficient and quality-assured results, even for sensitive
or demanding components.
Dirk Konzok, Sales Manager and Authorized Signatory at LPW:
„We have responded to the increased demand from our customers
for a simple semi-manual CNp ultrasound system that can do much
more than previous solutions. Now we are bridging the gap between
laboratory technology and near-production cleaning. The new LPW
product stands for a practical approach to high-quality cleaning of
complex geometries: powerful, flexible, and tailored to the requirements
of modern manufacturing processes.“
The system is particularly suitable for demanding tasks in areas
such as medical technology, additive manufacturing, or general industry.
Typical application fields include cleaning medical devices,
capillaries, and stents, de-powdering additively manufactured components,
and cleaning complex geometries after post-processing.
Additionally, pre- and intermediate cleaning processes in subtractive
manufacturing are possible.
The tanks have a capacity of 55
liters for cargo carriers up to Schäfer
size 2. (Photo: LPW)
Technical data overview:
The new LPW system is available for experiments
at the company‘s location in Riederich.
LPW Reinigungssysteme GmbH
Industriestraße 19
D 72585 Riederich
Telefon: +49 7123 38040
eMail: info@lpw-cleaning.de
Internet: http://www.lpw-cleaning.de
The control panel can be operated
intuitively, also via a tablet or smartphone.
(Photo: LPW)
- Floor space: approx. 2.2 m²
- Dimensions (D × W × H): 760 × 2,812 × 1,496 mm
- Connection power: 35 A / 15 kW
- Filter / heating circuit: approx. 1.2 m³/h
- Heating capacity: circuit approx. 3 kW, tank approx. 2 kW
- Ultrasound power: approx. 9 W/l
- Tank volume: 55 liters
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With the TDS501, E+E Elektronik introduces a next-generation dew point sensor. The sensor enables
continuous dew point measurement with auto-calibration without signal interruption, thereby
laying the foundation for reliable 24/7 process control.
TDS501 from E+E Elektronik: Continuous
dew point measurement down
to −70 °C Td without signal freezing
Industrial drying processes, especially in battery manufacturing, place the highest demands on dew point measurement.
At very low moisture levels, even the smallest deviations can affect product quality, yield and safety. This makes a stable,
continuous measurement signal essential. With the TDS501, E+E Elektronik presents its latest development for dew point
measurement: continuous measurement thanks to auto-calibration based on a new four-element measuring method, dew
point monitoring down to −70 °C Td, and smart protection concepts. The sensor therefore supports reliable around-theclock
process monitoring and efficient dehumidification control.
New: Four-element measuring method
Typical process events such as opening doors and airlocks or load
changes require a stable measurement signal. A frozen or heavily
averaged signal during auto-calibration can create blind spots in the
process in such environments. The TDS501 was therefore developed
around a key requirement in the control of very low dew points: auto-calibration
must not interrupt the measurement signal. In highly
dynamic applications, control decisions are made continuously. A
signal that freezes during calibration can conceal real process deviations
precisely when they matter most. To address this, the TDS501
uses an innovative new technology based on a four-element measuring
method with robust capacitive sensing elements. The
aim is to provide continuous dew point information for
24/7 process monitoring and therefore stable control
loops.
Dew point monitoring down to −70 °C Td
for demanding industrial drying
With the TDS501, E+E Elektronik extends its dew point portfolio
to measuring ranges down to −70 °C Td. This makes the sensor suitable
for applications in which extremely low moisture is a critical process
variable. These include battery manufacturing and the drying
of plastic granulate. In such processes, stable dew point monitoring
helps reduce moisture-related scrap, define safety
margins more precisely and control dehumidification
efficiently.
Smart protection concepts and
configurable filter caps
Seasonal fluctuations, plant shutdowns or component
failures can cause short-term condensation
in compressed air systems. The TDS501 is
designed to remain reliable even under such atypical
conditions and to reduce condensation-related
drift through practical design features. These include
robust sensing elements, a sintered stainless steel filter
and a durable stainless steel construction.
As standard, the TDS501 is equipped with a stainless
steel filter that offers a balanced ratio between protection and
response time. For cleanroom applications, where particularly
fast response times are required, an open filter cap is available as
an option. It further improves response time and allows even earlier
detection of dew point deviations.
Reproducible measurement results up to 80 bar
The TDS501 from E+E Elektronik.
(Photo: E+E Elektronik Ges.m.b.H.)
When dew point becomes a control variable, the measurement signal
must remain consistent even under changing operating conditions.
The TDS501 combines high repeatability with an accuracy of ±2
°C Td, supporting stable and reproducible production conditions. It
is also designed so that typical changes in process temperature do
not affect the measurement result.
With a pressure rating of up to 80 bar, the sensor can be installed
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directly where the process takes place. This provides a robust basis
for process control and quality assurance in industrial compressed
air application.
The TDS501 is more than a sensing element in a housing. It is a
holistically developed measurement system in which the sensing
element, electronics, mechanical integration, installation and adjustment
are optimally matched to one another. For users, this means
stable, repeatable measurement results and a reliable basis for
process decisions across devices, batches and operating conditions.
An optimally matched measurement system
for reliable performance
E+E Elektronik Ges.m.b.H.
Langwiesen 7
AT 4209 Engerwitzdorf
Telefon: +43 7235 6050 Telefax: +43 7235 6058
eMail: info@epluse.com Internet: http://www.epluse.com
SPETEC® Laminar Flow Boxes for Laboratory, Research, and Industry
A cleanroom exactly
where it is needed
rooms in these cases is often associated
with disproportionate structural and financial
effort.
With the Laminar Flow Box FBS, Spetec
offers a solution for the targeted creation
of local cleanroom conditions directly
at the workstation. The systems generate a
The requirements for particle- and germfree
work environments are continuously
increasing. Especially in laboratories,
research facilities, as well as in industrial
manufacturing and packaging. In many applications,
cleanroom conditions are only
needed locally. Building complete cleanuniform,
vertical laminar airflow, enabling
controlled air quality within a clearly defined
workspace.
Depending on the model variant, a Laminar
Flow Box FBS covers an effective
cleanroom area of approximately 0.37 to
1.12 sqm. HEPA filters of type H14 are used,
which filter out at least 99.995% of all particles
— based on a particle size of 0.12 μm
according to MPPS. This results in a significant
improvement in air quality compared to
the ambient air and creates the conditions
for cleanroom standards up to ISO Class 5.
The Laminar Flow Box FBS is available
in various sizes and can be used as both a
freestanding unit and a table version. The
construction is made exclusively from cleanroom-compatible
materials such as anodized
aluminum and acrylic glass. The
systems have been tested by the Fraunhofer
Institute for Production Technology and
Automation.
Thanks to its modular design, the Laminar
Flow Boxes can be flexibly integrated
into existing work environments — without
structural modifications and with minimal
installation effort.
Spetec Gesellschaft für Labor- und Reinraumtechnik
mbH
Am Kletthamer Feld 15
D 85435 Erding
Telefon: +49 8122 959090
Telefax: +49 8122 9590955
eMail: info@spetec.de
Internet: https://www.spetec.de
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For maximum flexibility
KEL-ERM VARIO from icotek:
Cable entry with variable
separation plates
The KEL-ERM VARIO is an advancement of the proven icotek cable entry system
and has been specifically designed for the entry of cables with and without connectors.
Different configurations can be easily implemented without replacing
the frame: With the plug-in separator bars, the frame can be individually adapted
to each application.
The KEL-ERM VARIO is easy and safe to
install. The modular system is based on a
clear structure and reduces the variety of
options to one frame size per version. Fewer
required components mean less storage and
procurement effort, while planning, design,
and assembly are simplified. For control cabinet
construction and device integration,
it offers additional flexibility. Thanks to the
variable filling, the KEL-ERM VARIO is suitable
for various requirements, from series
applications to customer-specific solutions.
Depending on the need, it can be equipped
with a different number of large or small
glands.
Automatic gland fixation
Depending on the gland used, cables with
diameters from 1 to 16 mm (single glands
KT1 to KT15) or 16 to 35 mm (single glands
KT16 to KT34) can be safely fed, sealed, and
strain-relieved. The cable glands are automatically
fixed in the frame during assembly.
After complete filling, the end cap is
securely screwed on. The KEL-ERM VARIO
is compatible with standard connectors for
10-, 16-, and 24-pin heavy-duty connectors.
The size KEL-ERM VARIO B is designed
for connectors measuring 46 x 46 mm (e.g.,
for controllers, counters). Thanks to the injected
seal and the use of single glands, the
high protection class IP65 is maintained
even with flexible configurations.
The advantages at a glance:
– Only one frame size for different
variants (e.g., 24|10, 24|7, 24|4)
– Maximum flexibility through plug-in
separator bars (included)
– High protection class IP65 thanks
to injected seal
– Maintains the integrity
of pre-assembled cables
– Quick retrofitting and easy
service work
– High packing density and a wide
variety of glands
– Strain relief according
to DIN EN 62444
– High stability and vibration resistance
– Very easy filling
– Compatible with IMAS-CONNECT
adapter glands
Less complexity, higher system
availability
The KEL-ERM VARIO allows processes to
be simplified, costs to be reduced, and the
entire product lifecycle to be optimized.
Optionally, the KEL-ERM VARIO is also
available with integrated threaded bushings
– perfect for mounting on the inside of enclosures
and ideal for vandalism protection
or unintentional loosening.
icotek GmbH
D 73569 Eschach
The new cable entry KEL-ERM-VARIO from icotek offers maximum flexibility in configuration. (Image: icotek GmbH & Co. KG)
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New sensor technology for autonomous cleaning robotics in dynamic operational environments
Cleanfix is the first company to rely on the
3D ultrasound sensor ADAR from Sonair
The Swiss manufacturer of professional cleaning systems
Cleanfix is the first OEM partner to integrate the 3D ultrasonic
sensor ADAR from the Norwegian company Sonair
into the new generation of its autonomous cleaning robot
RA660 Navi XL. The solution is designed for use in open
and shared environments.
Autonomous cleaning robots are increasingly part of regular operations
today – often unattended, at night, and in areas also used by
humans. They encounter changing conditions: limited visibility, moisture,
dust, as well as small or ground-level obstacles in their path.
Against this background, Cleanfix has specifically further developed
the perception systems of the RA660 Navi XL. A central component
is the 3D ultrasonic sensor ADAR, which enables reliable
obstacle detection even under conditions that are challenging for
optical or laser-based sensor systems.
“Our customers do not evaluate algorithms, but results,” says Roger
Kaiser, Head of Robotics at Cleanfix. “Stable operation, minimal
interruptions, and a system that works reliably for hours are crucial.
This is exactly where ADAR comes in – as a prerequisite to make
autonomous cleaning scalable in everyday life.”
“For Sonair, this integration is an important step towards broader
application of 3D ultrasound in robotics,” adds Knut Sandven,
CEO of Sonair. “Service robotics is one of the fastest-growing areas
of automation. At the same time, these systems are increasingly working
in environments shared with humans instead of isolated industrial
facilities. In such scenarios, robust environment perception is
essential for reliable and predictable operation.”
Reduced sensor technology through 3D ultrasound
instead of individual sensors
With ADAR, Cleanfix replaces multiple linear ultrasonic sensors
with a central 3D sensor unit. By bundling these into a single sensor,
system complexity and the number of components are significantly
reduced.
This directly impacts integration and operation: The 3D ultrasonic
sensor provides spatial environment data that supports navigation
and movement behavior in real time. As a result, the robot
reliably detects small or partially concealed obstacles at ground level
– such as bags, pallet edges, or tools, which are common in practice.
Data protection is also considered systemically: Since no imaging
data is recorded or stored, the robot can be used in sensitive
environments.
High availability through low-maintenance sensors
and stable operation
Since the RA660 Navi XL does not rely on optical sensor systems
with sensitive lenses, regular cleaning is unnecessary. This minimizes
downtime and service effort, increasing availability during daily
operation.
Furthermore, false interpretations (“false positives”), such as
caused by dust particles, occur much less frequently. As a result, the
RA660 Navi XL operates more evenly and with fewer interruptions,
directly impacting productivity and area coverage.
The operation is independent of ambient light, making it suitable
for use at night or in poorly lit areas.
Outlook: Safety certification for 3D ultrasound
In the future, the safety-oriented use of the technology is also gaining
importance: Sonair is currently working on a safety certification
according to PL d (ISO 13849) / SIL (IEC 61508). This represents an
important step for the use of 3D ultrasonic sensors in safety-critical
applications and addresses the increasing requirements for autonomous
systems in shared environments.
This integration into the cleaning robot RA660 Navi XL marks
a first step in the industrial application of Sonair’s 3D ultrasound
technology.
Sonair
N 0484 Oslo
(Copyright Cleanfix)
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Product Update BRXH: Optimized Lubrication, Better Sealing, More Precision
Rodriguez revises profile
rail guides for mechanical
engineering and robotics
Rodriguez now offers the profile rail guides of the BRXH series in an optimized version. The update includes three key
points: an expanded lubrication concept, a new sealing system, and higher precision. This makes processes even safer while
maintaining system compatibility.
Proven properties remain:
– Four ball rows in X arrangement with
45° pressure angle for load capacity
in all main directions
– Variants A, B, AL, BL, BS as well as
versions with and without flange
– Existing coatings still available
– Metal cover band usable
– Rail lengths up to 3,900 mm
– Interchangeability within a accuracy
and preload class
Higher accuracy becomes standard
Rodriguez GmbH now offers the BRXH series profile rail guides in an optimized version.
(Image: Rodriguez GmbH)
With the adjustments to its profile rail
guides BRXH, Rodriguez responds to the
increased demands in machinery construction
and automation. The fundamental
technical data remains unchanged, targeted
optimization steps increase process safety
and ensure longer service life and reproducible
precision.
More lubrication points
for uniform supply
The guide carriages now feature additional
lubrication points, through which the lubricant
is better and more evenly distributed
within the ball circulation unit. The systems
are still delivered pre-lubricated. When lubricating
from above, an adapter ensures
targeted distribution within the carriage.
New sealing concept
for demanding environments
A central element of the revision is the new
sealing system. Standardly, face seal double
lip seals and double lip longitudinal seals are
used, effectively protecting against particles
and contamination. Optional additional variants
are available: non-abrasive seal, additional
abrasive seal, and metal scrapers.
The previous normal accuracy class N is
eliminated. Instead, class H becomes the
new standard. The tolerances for height and
width have been reduced by approximately
50 percent compared to the previous N
version. Accuracy class P is now only available
upon request. The Z2 class in preload is
eliminated; Z0, Z1, and Z3 remain available.
Specifically, this means: higher repeatability
– especially relevant in robotics and automation
– and better parallelism, i.e., multiple
guides run more smoothly in parallel.
Other design adjustments
Additionally, the ground running surfaces of
the carriages have been increased from two
to three. For the rails, protective caps made
of plastic or optionally brass are available.
Rodriguez GmbH
D 52249 Eschweiler
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www.reinraum.de | www.cleanroom-online.com NEWSLETTER | Ausgabe DE 05-2023 Seite 71/103
Veranstaltungen im Mai 2026
Für mehr Informationen oder zum Anmelden einfach auf die Veranstaltung klicken
12.05.2026 Seminar Oberflächen in der Medizintechnik
Veranstaltungsort: Ostfildern, Veranstalter: Technische Akademie Esslingen e.V.
18.05.2026 - 20.05.2026 Symposium 2026 ISPE Annex 1 Symposium
Veranstaltungsort: Lyon (FR), Veranstalter: ISPE
19.05.2026 - 21.05.2026 Seminar Pharma-Ingenieur/in (PT 25) - Block I
Veranstaltungsort: Mannheim, Veranstalter: CONCEPT HEIDELBERG GmbH
19.05.2026 - 19.05.2026 Workshop Performance Workshop Reinraum-Praxis
Veranstaltungsort: Reinraum Training Ceneter Frankfurt, Veranstalter: Cleanroom Future GmbH
20.05.2026 - 21.05.2026 Tagung 16. Fachtagung: Technische Sauberkeit in Montage- und Produktionsprozessen
Veranstaltungsort: Heidenheim, Veranstalter: Ultima Media Germany GmbH
20.05.2026 Seminar Praxis-Seminar für neue Teammitglieder: Kontaminationskontrolle und Arbeiten im Reinraum
Veranstaltungsort: München, Veranstalter: comprei Reinraum-Handel und Schulungs GesmbH
Veranstaltungen im Juni 2026
Für mehr Informationen oder zum Anmelden einfach auf die Veranstaltung klicken
02.06.2026 Seminar GMP-News 2026
Veranstaltungsort: Rheinfelden (CH), Veranstalter: Swiss Cleanroom Concept GmbH
04.06.2026 Webinar Annex 1 - Erfahrungen und Praxisbeispiele
Veranstaltungsort: Online, Veranstalter: PTS Training Service
09.06.2026 - 10.06.2026 Seminar Life Science Ready Days 2026
Veranstaltungsort: Karlsruhe, Veranstalter: Systec & Solutions GmbH
09.06.2026 - 10.06.2026 Seminar Fachgerechte Verlegung von nora Kautschukböden: Unterboden bei Wandbelägen &
Abdichtung von Nassbereichen
Veranstaltungsort: Weinheim, Veranstalter: nora systems GmbH
10.06.2026 - 11.06.2026 Seminar Bestimmung von Messunsicherheiten nach GUM
Veranstaltungsort: Hamburg, Veranstalter: Testo Industrial Services GmbH
10.06.2026 - 11.06.2026 Training & Schulung GMP-Reinraumschulung für aseptische Bereiche
Veranstaltungsort: Osnabrück, Veranstalter: Piepenbrock Dienstleistungen GmbH + Co. KG
11.06.2026 - 12.06.2026 Seminar Environmental Monitoring - Compliant and Reasonable
Veranstaltungsort: Kopenhagen, Veranstalter: CONCEPT HEIDELBERG GmbH
11.06.2026 Seminar Hygiene
Veranstaltungsort: Affoltern am Albis, Veranstalter: PTS Training Service
www.reinraum.de | www.cleanroom-online.com NEWSLETTER | Ausgabe EN 05-2026
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Veranstaltungen im Juni 2026
Für mehr Informationen oder zum Anmelden einfach auf die Veranstaltung klicken
15.06.2026 - 19.06.2026 Seminar Kalibriertage Thermodynamik: Prüfmittelmanagement und Kalibriertraining
Veranstaltungsort: Kirchzarten bei Freiburg, Veranstalter: Testo Industrial Services GmbH
16.06.2026 - 18.06.2026 Webinar GMPs for Equipment, Utilities and Facilities - Live Online Training
Veranstaltungsort: online, Veranstalter: CONCEPT HEIDELBERG GmbH
16.06.2026 - 17.06.2026 Seminar Klinische Prüfung mit Prüfpräparaten: GMP / GDP bei der Herstellung und Logistik
Veranstaltungsort: Alzenau/Digital, Veranstalter: PTS Training Service
17.06.2026 Seminar Aktualisierung und Auffrischung für Reinraum-Servicetechniker/-innen Neues in der
Mess- und Gentechnik, GMP & Co.
Veranstaltungsort: Krefeld, Veranstalter: IHK Mittlerer Niederrhein
17.06.2026 - 19.06.2026 Seminar Validierungsbeauftragte/r in der pharmazeutischen Industrie (QV 16)
Veranstaltungsort: Hamburg, Veranstalter: CONCEPT HEIDELBERG GmbH
17.06.2026 - 17.06.2026 Webinar PUPSIT - Erwartung & Umsetzung - Live Online Seminar
Veranstaltungsort: online, Veranstalter: CONCEPT HEIDELBERG GmbH
18.06.2026 Seminar GCP ICH E6 R3 und EMA Guidelines - Computersystemvalidierung und Datenintegrität
Veranstaltungsort: Siegburg, Veranstalter: PTS Training Service
23.06.2026 - 25.06.2026 Seminar Pharma-Ingenieur/in (PT 25) - Block II
Veranstaltungsort: Hamburg, Veranstalter: CONCEPT HEIDELBERG GmbH
23.06.2026 Seminar Räume, Luft und Technik: Gestaltung und Qualifizierung von Räumen
Veranstaltungsort: Online, Veranstalter: PTS Training Service
24.06.2026 Seminar Räume, Luft und Technik: Lüftungsanlagen
Veranstaltungsort: Online, Veranstalter: PTS Training Service
25.06.2026 Seminar Schleusenkonzepte im Reinraum: GMP-Praxis erleben mit 3D-Simulation
Veranstaltungsort: Online, Veranstalter: PTS Training Service
25.06.2026 Seminar Räume, Luft und Technik: Messtechnik, Umsetzung gemäß Annex 1 neu und DIN ISO 14644
Veranstaltungsort: Online; Veranstalter: PTS Training Service
25.06.2026 - 26.06.2026 Tagung 34. Fachtagung „Industrielle Bauteilreinigung“
Veranstaltungsort: Esslingen; Veranstalter: Fachverband industrielle Teilereinigung (FiT) e.v.
30.06.2026 - 01.07.2026 Webinar Annex 1 Intensive Training Course - Live Online Training
Veranstaltungsort: online; Veranstalter: CONCEPT HEIDELBERG GmbH
Impressum:
W.A. Schuster GmbH / reinraum online · Mozartstraße 45 · D 70180 Stuttgart · Tel. +49 711-9640350 · Fax 9640366
info@reinraum.de · www.reinraum.de · GF Dipl.-Designer Reinhold Schuster · Stgt, HRB 14111 · USt.-IdNr. DE 147811997
Originaltexte und Bilder:
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