Newsletter_07-2026_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 07/26
Paperless
labelling
with VEYA
in a cleanroom
Quelle: AdobeStock 40914936
TITLE
With VEYA, cleanroom equipment is also digitally labeled in a revision-safe manner.
(Image credit: Stormbit GmbH)
VEYA displays in real-time what matters
on-site in the cleanroom. LCDbased
MODI dashboard: The VEYA
app centrally controls which information is to be displayed in
real-time at which cleanroom. (Image credit: Stormbit GmbH)
Error-free operation in the cleanroom
has the highest priority
Paperless labeling
with VEYA
from Stormbit
In GMP-compliant cleanroom production, the highest accuracy,
purity, and safety are top priorities. Nevertheless,
many documentation processes and labeling requirements
are still carried out on paper—and thus remain susceptible
to errors and inconsistencies. An increasing number of
pharmaceutical manufacturing facilities and laboratories
are therefore turning to paperless solutions to make their
processes more efficient and secure.
VEYA comes from Stormbit, a software solutions company of the
Systec & Solutions Group. The system enables paperless, GMPcompliant
labeling and visualization of production-relevant data
in the cleanroom environment. Central information such as production
data, room parameters, status messages, or cleaning states
are displayed in real time via LCD-based HMIs (for example, MODI
dashboards) and ePaper-based labels (LSLs; LSL = Life Science Label)
and the corresponding app. The human factor as a source of error
is eliminated. This precise communication increases production
safety and enhances efficiency.
VEYA visualizes all relevant KPIs and parameters—from room
temperature, pressure, humidity, cleaning status, to all order-related
production data. This ensures that all decision-critical information
is available in real time inside and outside the cleanroom. The systems
can be integrated firmly into the cleanroom wall as needed or
be mounted flexibly on containers or production equipment.
The underlying data are typically already available digitally in
existing enterprise systems. VEYA accesses this information directly
and transmits it to the LCD panels or MODI dashboards and ePapers
installed outside the cleanrooms. There, they are clearly structured,
displayed in the company‘s corporate design, and optimally legible.
Unlike traditional paper displays, the presentation is based on a unified,
validated data source—reliable avoidance of conflicting or outdated
information.
Which information is displayed on which LCD panel and label
can be conveniently controlled via the central VEYA app.
The MODI dashboards are specifically designed for use under
GMP conditions and in cleanrooms and are ideal for visualizing
room information as well as for building automation applications.
The fanless 7“ and 10.1“ LCD displays with LED backlight technology
feature an intuitive multi-touch display with optical bonding, which
can be reliably operated even with cleanroom gloves. Thanks to IPS
panels with up to 178° viewing angles and various interfaces such as
USB, Gigabit Ethernet, WLAN, and Bluetooth, the devices can be
flexibly integrated into existing infrastructures. Optional features include
pre-installed kiosk mode and various mounting and enclosure
options—including IP65 versions.
With the ePaper-based labels (LSLs), the manufacturer also offers
the possibility to remove paper from process containers, production
batches, and laboratory equipment. E-Paper labels, which
are attached instead of paper tags to devices and objects, also draw
their data from the central VEYA app. This ensures that labels on cleanroom
equipment are audit-proof and always up to date.
The LSLs have also been specifically developed for the life
sciences industry. The devices are available in 4.2“ and 7.5“ sizes and
feature a four-color e-paper display (black, white, red, yellow). They
meet the IP65 protection class and are designed for optimal cleanability—a
crucial factor in cleanroom environments. An integrated
multi-color LED with edge-light provides quick visual status recognition.
Connectivity is wireless via the LSL access point, while the
battery operation allows up to five years of runtime. The solution is
ideal for semi-static digital labeling applications and offers various
mounting options—both with magnetic and non-magnetic mounts,
which can be individually adapted to different use cases.
This innovative solution from Stormbit is agile, flexible, and
quickly adaptable, offering maximum data security. The company
initially specialized in life-science-ready solutions for the pharmaceutical
industry and supports pharmaceutical production and laboratories
from GMP-compliant planning to the implementation of
HMI systems with VEYA and validated data transfer.
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
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Reading
made
easy at
www.reinraum.de
JULI 2026
Dear cleanroom professionals,
“Nothing is good unless you do it”
– this famous quote by Erich Kästner (1950)
cannot always be expected to apply to football, nor
indeed to politics, because, of course, everyone
defines ‘good’ according to their own feelings.
I think we’ve put together another really good
newsletter for you. You can find a brief overview of
the contents of this newsletter here:
> Paperless labeling with VEYA from Stormbit
> A chapter comes to an end
> Ilmac Lausanne 2026 puts the laboratory of the
future, AI and biotools centre stage
> Innovation meets practice:
POWTECH TECHNOPHARM takes centre
stage for processing technology again in 2026
> Cleanroom with 100% energy recovery from
the back process
> Fraunhofer FEP opens
biosafety level 2 laboratory
> Calibration as a key factor in process efficiency
> . . .
Kind regards
Reinhold Schuster
All content has been translated using AI.
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Des informations désormais disponibles dans votre langue maternelle
Információk most már az Ön anyanyelvén
Informacje teraz w Twoim języku ojczystym
Informace nyní ve vašem rodném jazyce
Informazioni ora nella tua lingua madre
Información ahora en tu lengua materna
Informatie nu in uw moedertaal
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How cleanrooms are inspired by the automotive industry
Configure-to-Order Plus (CTO+)
From Engineer-to-Order to
Configure-to-Order Plus
In 2024, ABN Cleanroom Technology redefined
the cleanroom industry by introducing
ADAPTUS, the world‘s first product platform
strategy for cleanroom engineering. By
organizing critical cleanroom components
into pre-engineered and validated building
blocks, ABN shifted the industry from traditional
Engineer-to-Order delivery toward a
smarter, faster, and more predictable model:
Configure-to-Order Plus.
Configure-to-Order Plus is the framework
that governs how ADAPTUS is applied,
ensuring that speed, reliability, sustainability,
and budget control are delivered together
on every project, without compromise.
This matters because the cleanroom
industry has long operated on a set of assumptions
that force project teams into difficult
choices. Faster delivery is assumed to
increase risk.
Tighter budgets are believed to limit longterm
performance. Custom engineering is
treated as the only path to compliance. These
assumptions are not laws. They are the
product of a delivery model that was never
designed to do better.
CTO+ was built on the rejection of these
assumptions. By embedding performance
guarantees into the architecture of the
ADAPTUS platform itself, rather than managing
them through project procedures,
CTO+ ensures that no configuration ever
compromises what matters most to a client,
regardless of which priority drives the project.
This whitepaper explains what Configure-to-Order
Plus is, how it works, and why
it removes the trade-offs that have defined
cleanroom projects for decades.
Still engineering from scratch in 2026?
Most cleanroom projects across the industry
are still delivered using an Engineer-to-Order
(ETO) approach. In this model, each cleanroom
is designed and engineered largely
from scratch, tailored to the specific requirements
of an individual project. While this
allows for a high degree of customization, it
also introduces structural inefficiencies that
compound across the project lifecycle.
In an ETO approach, design decisions
are made sequentially and are tightly interconnected.
A change in one part of the
design triggers a cascade of changes elsewhere.
Key performance characteristics only
become fully visible late in the process, making
outcomes difficult to predict, validation
complex, and trade-offs apparent only after
critical decisions have already been locked
in.
As cleanroom environments became more
complex and more regulated, these limitations
became increasingly consequential.
Faster time to market, consistent validation,
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and into platform development, embedding
knowledge, validation, and performance
into the system itself. The result is lead
times starting from as little as six weeks,
cost savings of up to 20%, and predictable
cleanroom behavior before construction
and commissioning begin.
The role of the platform:
A Lesson from the Automotive Industry
Vangelabbeek Tom
Van Walleghem Olivier
Nelissen Jo
To understand how a platform-based approach
can protect critical values across different
cleanroom configurations, the automotive
industry offers a useful parallel.
To make it clear, consider one example
of how the Volkswagen Group deploys shared
platforms across its brands. The Audi S3
and the Volkswagen Golf, two vehicles from
different brands within the same group, are
both built on the same MQB platform. The
Audi S3 is configured for speed and performance.
The Volkswagen Golf is configured
for comfort, everyday usability, and practicality.
Their driving dynamics, interior refinement,
and feature sets differ substantially.
Yet both meet the same safety and regulatory
standards, regardless of how each is configured
or what market it serves.
and predictable performance over the full lifecycle
could no longer be reliably achieved
through one-off engineering alone.
At ABN Cleanroom Technology, this reality
led to an early and deliberate shift. Rather
than refining the ETO model, ABN moved
to a fundamentally different approach:
Configure-to-Order Plus.
From engineering to configuration
In CTO+, cleanrooms are not engineered
from scratch. They are configured from preengineered
and validated building blocks
developed as part of an integrated system
architecture. These building blocks, ranging
from air handling units and wall panel systems
to filtration modules and humidifiers,
are designed, tested, and validated in advance,
with defined interfaces and known
performance characteristics. Cleanrooms
are configured by combining proven components
within this architecture, rather than
being designed element by element for each
individual project.
This shift fundamentally changes where
complexity is managed. Engineering effort
moves away from individual projects
Configuration is used to emphasize different
characteristics, such as performance or
cost efficiency, but never to remove or weaken
the critical fundamentals defined by the
platform. Variability is permitted only where
it does not affect global system behavior.
The key insight this example provides is
straightforward: by fixing critical fundamentals
at the architectural level, the platform
defines clear boundaries within which configuration
is allowed. Different configured
outcomes remain predictable precisely because
the platform prevents variability where
it matters most.
ABN Cleanroom Technology applies
this same logic to cleanroom delivery
through the ADAPTUS platform and the
Configure-to-Order Plus framework. The
building blocks of ADAPTUS function like
the shared architecture of an automotive
platform, pre-engineered and validated
across every configuration. Two examples
illustrate this directly.
ICONIC is a cleanroom configured for
speed. It is designed for organisations where
time to market is the primary driver, delivering
a fully validated, operational cleanroom
in the shortest possible lead time. INTEGRA
is a cleanroom configured for energy efficiency
and long-term lifecycle performance.
It is the choice for organisations where sustainability
and total cost of ownership take
priority over delivery speed.
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Despite their different emphases, ICONIC,
INTEGRA, and all other configurations are
governed by the same guaranteed performance
levels, referred to as the Olympic
Minimum, that ABN‘s leadership defines
and the ADAPTUS platform enforces. This
means no client choosing ICONIC accepts
a compromise on reliability. No client
choosing INTEGRA accepts a compromise
on speed. The platform protects what is not
chosen just as rigorously as it delivers what
is.
This is the distinction that separates
Configure-to-Order Plus from conventional
approaches. Clients do not negotiate between
priorities. They define what matters
most, and the platform protects everything
else.
Configure-to-Order Plus: The
ABN Cleanroom Technology Framework
Within CTO+, speed, reliability, sustainability,
and budget control are treated as nonnegotiable
system fundamentals. Before any
configuration takes place, ABN‘s leadership
defines the guaranteed performance levels
that must be maintained across all four values
in every project. These levels are referred
to as the Olympic Minimum.
The Olympic Minimum is not a contractual
commitment made on a projectby-project
basis. It is embedded directly into
the architecture of the ADAPTUS platform,
meaning it is enforced by the system itself
rather than by individual project decisions
or procedures. Within this framework, no
configuration, regardless of its primary focus,
ever falls below the Olympic Minimum
across the remaining values. The platform
architecture prevents it.
In most cleanroom projects across the
industry, speed, reliability, sustainability, and
budget control are treated as competing objectives.
Faster delivery is assumed to reduce
reliability. Tighter budgets are believed to limit
long-term performance. CTO+ is built on
the rejection of these assumptions.
LEGOlization: One platform, multiple configurations
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CTO+ redefines the sequence of decisionmaking.
Before configuration begins, it is
made explicit which value must take priority
based on the client‘s needs. The remaining
values are then protected at platform level
through the ADAPTUS library of pre-engineered,
validated building blocks.
The client‘s priority value drives configuration
choices. The other three values are
never compromised in the process.
This is the distinction that separates
Configure-to-Order Plus from conventional
Configure-to-Order approaches. Standard
CTO uses standardization to improve efficiency
and reduce lead times. CTO+ goes
further by ensuring that standardization
never comes at the cost of critical values,
regardless of which priority a client selects.
Values are protected before configuration
begins, not corrected after problems emerge.
Defining the Four Values
Speed
Speed describes how quickly a cleanroom
can be delivered into validated operation.
It is measured as the time span between
contract signature and validated handover
to operations. When speed is selected as
the primary value, configuration decisions
are oriented toward minimizing total project
lead time across design, construction, and
commissioning, without compromising the
Olympic Minimum for reliability, sustainability,
or budget control.
Reliability
The cleanroom industry has been engineering from scratch for decades, and
the inefficiencies have become invisible simply because they were accepted
as normal. At ABN, we refused that premise. With Configure-to-Order Plus
and the ADAPTUS platform, we shifted complexity away from individual
projects and embedded it once, at platform level, where it compounds in
value over time. Every cleanroom we deliver inherits validated performance
from day one, not because we engineered it again, but because we engineered
it right the first time. This is not an incremental improvement on how
cleanrooms are built. It is a fundamentally different starting point, and it
changes what clients can expect from a cleanroom partner.“
Jo Nelissen
CEO / Founder ABN Cleanroom Technology
Reliability describes the ability of the cleanroom
system to deliver stable and predictable
performance throughout its operational
life. When reliability is selected as the primary
value, configuration focuses on architectural
robustness through redundancy at
both component and subsystem level.
Continuous monitoring is provided
through CleanConnect, ABN‘s IoT platform
for ISO cleanrooms, and GMP-Connect,
its equivalent for GMP-regulated environments.
Together with the VIX system,
ABN‘s dedicated reliability architecture,
these platforms target 99.99% operational
uptime, as documented across ABN‘s operational
cleanroom portfolio.
Sustainability
Sustainability describes how the cleanroom
performs over its full lifecycle rather than at
a single point in time. When sustainability is
selected as the primary value, configuration
decisions are driven by total lifecycle performance.
The focus lies on energy efficiency,
the use of durable and sustainable materials,
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and optimization of total lifecycle cost, ensuring
long-term environmental and economic
resilience.
Price
Budget control describes the upfront investment
required to deliver a compliant and
fully operational cleanroom. When budget
control is selected as the primary value, configuration
decisions focus on minimizing
initial capital expenditure while delivering
all required performance and compliance
standards. This means achieving the lowest
possible upfront investment while remaining
fully within the Olympic Minimum for
speed, reliability, and sustainability.
ADAPTUS and Value Engineering:
Making CTO+ Operational
Making Configure-to-Order Plus operational
requires more than a framework. It
requires a system in which value priorities
and guaranteed performance levels are
translated into executable decisions and
enforced consistently throughout the project
lifecycle.
At ABN Cleanroom Technology, this is
achieved through the ADAPTUS platform.
ADAPTUS is a cleanroom product platform
built from pre-engineered and validated
building blocks. Each building block
is developed as part of an integrated architecture,
with known interfaces and defined
performance characteristics. Performance
is embedded at platform levels and reused
consistently across projects, rather than
being re-established for each individual cleanroom.
All building blocks meet ISO 14644
and applicable industry standards including
GMP Annex 1.
Every building block within ADAPTUS
is designed to meet or exceed the Olympic
Minimum across all four critical values.
The Olympic Minimum is not a contractual
commitment applied after the fact, it is embedded
into the architecture of the platform
itself, making performance below this threshold
architecturally impossible from the
moment configuration begins.
Value engineering is applied only after
value priorities have been established and
the Olympic Minimum is already met. It is
used to compare and refine configuration
options within these protected boundaries.
Improvements in efficiency, cost, or complexity
are pursued only where they do not
undermine the defined performance levels.
Optimization is deliberate and controlled,
never reactive.
This sequencing is critical. By placing
value engineering after value definition and
performance protection, CTO+ ensures that
the drive for efficiency never introduces
unintended trade-offs.
Verification extends beyond design and
delivery into operation. Through CleanConnect
for ISO cleanrooms and GMP-Connect
for GMP cleanrooms (developed by our sister
company Smartlog), cleanroom performance
is continuously monitored against
the defined baselines. This provides ongoing
assurance that guaranteed performance
levels are consistently met throughout the
lifecycle, not only at the point of handover.
Operational data gathered through these
platforms does not serve only as a verification
record. This data feeds back into
the ADAPTUS platform, strengthening validation
evidence, refining performance assumptions,
and enabling continuous improvement
of the building blocks themselves.
Through this integrated approach, Configure-to-Order
Plus becomes enforceable,
verifiable, and repeatable across every project.
Trade-offs below the Olympic Minimum
are not controlled through procedures
or prevented through experience. They are
made architecturally impossible.
The result is a platform that becomes
more precise, more validated, and more reliable
with every cleanroom delivered.
Conclusion: The Cleanroom
Trade-Off Is a Lie
Configure-to-Order Plus changes what clients
can expect from a cleanroom partner.
Through the VIX system and ADAPTUS
platform, ABN delivers cleanrooms with
lead times starting from six weeks, operational
uptime of 99.99%, cost savings of up
to 20% compared to traditional Engineerto-Order
approaches, and full compliance
with ISO 14644 and GMP Annex 1 from day
one. These are not project-specific achievements.
They are platform-level outcomes
that every client inherits by default.
Beyond the numbers, CTO+ changes
the nature of the client relationship itself.
Clients no longer need to negotiate between
priorities or accept that choosing speed means
accepting risk elsewhere. They define
what matters most, and the system protects
everything else. Decisions that previously
required trade-offs now require only clarity
about priorities.
For industries where downtime, noncompliance,
or cost overruns carry serious
consequences, this is not a marginal improvement.
It is a fundamentally different basis
on which to commission, operate, and expand
a cleanroom facility.
ABN Cleanroom Technology delivers
cleanrooms that are faster, more reliable,
more sustainable, and more cost-controlled,
not as a choice between these qualities, but
as a guaranteed combination of all four.
ABN Cleanroom Technology NV
BL 3740 Munsterbilzen
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A chapter comes to an end
Norbert Otto concludes his active role at SwissCCS
For many years, Norbert Otto was part of
the SwissCCS association. It was not easy
for him to say goodbye to his active role.
After over 30 years in the SwissCCS association,
the moment had come. „At 71 years
old, this step is not entirely easy—and yet it
feels right,“ says Norbert Otto. His connection
to SwissCCS, or previously SRRT, dates
back to 1994 when he founded his company
in Germany with a Swiss business partner.
What initially began with curiosity and professional
interest quickly developed into a
deep bond with the people and the topics
of cleanroom technology that characterize
this community. Over the years, he has witnessed
not only the development of the field
but also SwissCCS itself evolving into a platform
for international exchange, inspiration,
and collegial cooperation.
What he remembers most are the people:
working together, striving for good solutions
during meetings on standardization
both nationally (SNV, VDI, DIN) and internationally
(ISO Committee). The conversations
on the sidelines of events, such as the
numerous training sessions on cleanroom
technology, which embody the trust and reliability
of the association. This also includes
his time as interim president, during which
the association placed great trust in him.
„Much has changed over these years—in our
environment, in our field, and even within
the association itself. And yet, one thing has
remained: the spirit of collaboration,“ says
Norbert Otto.
Three decades are more than just a long
period of time. They stand for encounters,
developments, engagement, and many
shared experiences. When he joined back
then, he could not have imagined the place
SwissCCS would eventually hold in his life.
The association became much more than
a professional network for him—it was for
many years a piece of home.
As he ages, perspectives shift. What was
once taken for granted now requires more
strength and time. Therefore, he feels the
time has come to pass on responsibility
and create space for new ideas and younger
voices.
Norbert Otto will, even as he withdraws
from active participation, remain connected
to the association. „I wish SwissCCS
continued lively development, committed
members, and the courage to preserve what
works while also daring to try new things,“
says Norbert Otto at the farewell event.
C-tec
Cleanroom-Technology GmbH
Tübinger Straße 47
D 72127 Kusterdingen
Telefon: +49 7071 6887180
Telefax: +49 7071 688718700
norbert.otto@c-tec.de
http://www.c-tec.de
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Ilmac Lausanne 2026 puts
the laboratory of the future,
AI and biotools centre stage
On 23 and 24 September 2026, Expo Beaulieu Lausanne
will become the meeting point for Switzerland’s chemistry
and life sciences sector. Ilmac Lausanne 2026 is expected
to attract around 200 exhibitors and 3,500 trade visitors.
At its core will be a conference programme featuring
over 70 presentations and pitches, together with the Future
of Life Sciences - Area, which will address key future topics
including Process Analytical Technology, biotools, artificial
intelligence, quantum computing and the laboratory of the
future.
In recent years, Ilmac Lausanne has established itself as a focused
platform for the French-speaking Swiss chemistry and life sciences
industry. In 2026, it will demonstrate how laboratory and process
technology, automation, digitalisation and industrial applications
are continuing to evolve along the entire value chain. The event thereby
positions itself as more than a conventional laboratory trade
fair, serving instead as an industry meeting point for research, industry,
start-ups and technology partners.
“The requirements placed on laboratories, production and development
are changing rapidly. At Ilmac Lausanne we bring together the
players who are actively shaping this transformation – from PAT and
automation to AI, biotools and new forms of collaboration,” explains
Céline Futterknecht, Exhibition Director Ilmac. “We are deliberately
setting new standards – in terms of content, format and the way we
combine networking with knowledge transfer.”
Conference programme unites Swiss expertise with international
impetus The accompanying conference forms the content hub of
the event. It bridges scientific excellence and concrete industrial
application. On both days, visitors can look forward to more than 70
presentations and pitches, curated by renowned partners. National
and international top speakers will provide insights into current developments
and future topics.
Day 1 will focus on Process Analytical Technology (PAT). Under the
leadership of the Swiss Chemical Society (SCS) in cooperation with
the Swiss Process and Chemical Engineers (SGVC), the emphasis
will be on quality assurance, AI integration and industrial applications.
Day 2 will be devoted to biotools and the Swiss life sciences
ecosystem. Led by BioAlps, the Canton of Vaud and InnoVaud, the
programme will show how bioconvergent technologies and strong
partnerships translate innovation from research into application.
Future of Life Sciences - Area: experiencing innovation
The Future of Life Sciences - Area will showcase concrete applications
in automation, artificial intelligence, laboratory planning and
industrial digitalisation. The curated platform combines showcases,
expert contributions, and dialogue formats to explore how research,
production, and patient care could evolve by 2040.
The area is being realised in close collaboration with partners from
the Swiss life sciences ecosystem, including Siemens, HDI, laboratory
planner Tonelli and other leading industry players. Together
they will demonstrate how automation, artificial intelligence and industrial
applications interact in practice, in a tangible and experiential
way. With Brett Staahl (Co-Founder and VP External Innovation,
Scribe Therapeutics) from the USA, the programme also gains an
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international perspective from the life sciences sector. Both days
will focus on central future questions for the industry:
– Day 1: Laboratory of the Future
The transformation of modern laboratories from standalone facilities
into networked, data-driven high-performance platforms will
take centre stage. Topics such as automation, new working methods
and digital processes will illustrate how speed, quality, and competitiveness
will change in the future. What does this mean for Switzerland,
and what should companies do now to secure their competitive
edge?
– Day 2: AI & Quantum Computing
The second day will examine the impact of artificial intelligence,
quantum technologies and advanced automation across the entire
life sciences value chain – from research and development through
production and regulation to patient interaction. The focus will
be on how these technologies are already transforming processes,
decisions and collaboration throughout the ecosystem today. The
discussion will again address what this means for Switzerland and
what companies should do to remain competitive.
“The life sciences industry is part of Switzerland’s DNA. To secure
its long-term international competitiveness, the digital transformation
along the entire value chain plays a central role – precisely
these developments are made tangible in the Future of Life Sciences
- Area,” says Jens Feddern, Head Vertical Market Life Science,
Siemens Switzerland Ltd.
Space for exchange and new connections Ilmac Lausanne deliberately
creates space for a wide range of encounters. Whether in the
Speakers Corner, the Startup Area or formats such as “Women in
Life Sciences”, the event thrives on personal exchange and the setting
of pioneering impulses.
The daily Networking Lunch and the Networking Apéro on the first
exhibition day foster inspiring conversations and new contacts,
made possible by Endress+Hauser as Networking Partner and an environment
deliberately focused on quality, dialogue and networking.
The Apéro is also realised in cooperation with Apin. Both events
are included in the ticket price and are popular networking occasions
for both visitors and exhibitors. Additional culinary highlights
are provided by barista partner VITARIS and gelato partner Milian,
rounding off the exhibition experience.
Swissness as a foundation Ilmac Lausanne combines Swiss quality,
innovative strength and international relevance. It stands for
exquisite, personal networking in a compact two-day format, embedded
in one of Europe’s strongest life sciences regions. As the
leading platform in French-speaking Switzerland, it complements
Ilmac Basel, which serves as the largest specialist trade fair for the
chemistry and life sciences industry in Switzerland and represents
the international highlight. “In Lausanne, personal encounters and
new partnerships are formed, while Basel provides the international
stage for the sector. This interplay is what makes Ilmac unique,” says
Futterknecht.
With Ilmac 365, the industry remains connected throughout the
year. Before and during the fair, the platform acts as a personal event
assistant, supporting individual visit planning and complementing
the live experience with digital networking and information offerings.
The full agenda, exhibitors and further information on the
event are available at any time on www.ilmac.ch/365 and via the app.
ILMAC
MCH Messe Schweiz (Basel) AG
Messe Basel
4005 Basel
Schweiz
Telefon: +41 58 206 3106
eMail: anne.klipfel@ilmac.ch
Internet: http://www.ilmac.ch
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For 2 consecutive years, the processing community has been heading to Nuremberg.
POWTECH TECHNOPHARM is getting ready for the next round:
from September 29 to October 1, 2026, everything will revolve around technologies
for processing powders, solids, and Liquids.
Innovation meets practice:
POWTECH TECHNOPHARM takes centre stage
for processing technology again in 2026
POWTECH TECHNOPHARM has drawn the processing community to Nuremberg
two years in a row. Now it’s preparing for the next round: From 29 September
to 1 October 2026 the Nuremberg exhibition venue will once again be abuzz
with everything relating to the processing of powders, solids and liquids, with a
focus on the latest market and trend topics. The international processing community
can look forward to three full days of top-level expert interaction, innovations
and trends for the relevant sectors of the process engineering industry.
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With just a few months to go before the exhibition, the team from
POWTECH TECHNOPHARM is putting every effort into the preparations.
Although the exhibition starts at the end of September,
the current floor plans can already be viewed online. “The Cross Industry
trade fair offers ideal opportunities. Companies looking to tap
into new markets and generate additional leads should secure an exhibition
space now – together we will find a suitable space,” says Marianny
Eisenhofer, Director POWTECH TECHNOPHARM. “We are
looking forward to bringing together the many sectors that make up
the processing community again in September, and to showcasing
POWTECH TECHNOPHARM as the heart of the process engineering
industry.” Survey results gathered by an independent institution
show that in 2025, 96 percent of the surveyed exhibitors were able to
make new business connections and expected a positive impact on
business. Likewise, 96 percent of the visitors surveyed had an optimistic
view of the future and were satisfied with their visit to POW-
TECH TECHNOPHARM 2025.
This year’s POWTECH TECHNOPHARM will be held in the centrally
located Halls 7A to 9 at the Nuremberg exhibition venue. These
are ideally located for easy access from the metro station as well as
the Mitte and the large Ost parking areas. Once again, the exhibition
ticket this year will include the VGN KombiTicket for local public
transport. That means both exhibitors and visitors can enjoy free,
environmentally friendly travel to and from POWTECH TECHNO-
PHARM by metro, tram, bus and regional rail within Nuremberg and
some surrounding areas.
Practical knowledge and a broad spectrum of businesses
The international community for process engineering meets in Nuremberg
in autumn to introduce the latest technologies and futureoriented
innovations, to interact with each other and also to discuss
and tackle the challenges and opportunities relating to all aspects
of processing powders, solids and liquids. Analysing, size reduction,
screening, mixing, conveying, storing, dosing and compacting … dynamic
processes are everywhere in process engineering. In addition
to mechanical, thermal and analytical processes, this also includes
methods for processing materials in liquid or paste form and bulk
solids together. POWTECH TECHNOPHARM is the international
platform where exhibitors can present the latest product innovations
and services in process engineering to the key sectors in the
industry.
Once again this year, the exhibition halls will be the place to meet
long-familiar exhibitors as well as first-timers who are adding to the
wide range of technology products and services used for processing
in every sector. Developers, heads of production, decision-makers
and buyers from various sectors including foodstuffs, the chemical,
pharmaceutical and recycling industries and explosion protection
particularly appreciate the ability to engage with their peers
on technical questions: Processes, machines and components can
be experienced first-hand, with the focus on professional guidance
on selecting innovations and practicable solutions for individual
problems. POWTECH TECHNOPHARM enables visitors from all
sectors to think beyond the box, experience technological diversity,
pick up ideas from adjacent sectors and discover unexpected inspirations.
Focus on market and trend topics
Sustainability and the circular economy are a key focus in all segments
of the process industry right now. There is also a focus on
expanding the automation and digitalization of production. POW-
TECH TECHNOPHARM 2026 will provide a dedicated space for
these themes, which will include special display areas. “Our pavilions
provide exhibitors with an uncomplicated opportunity to participate
in the exhibition, and the way themes are clustered attracts a
high level of visitor attention,” asserts Eisenhofer. She explains further:
“The key aspects are networking and more in-depth interaction
with experts. You’ll find innovative first-time exhibitors, smaller
firms and newcomers to process engineering, all in the same place.”
The following pavilions are planned for POWTECH TECHNO-
PHARM 2026: Pharma in Focus, Recycling in Focus, Smart Industry
in Focus and the Processing Alliance pavilion representing the global
network of leading trade fairs in the NürnbergMesse Group. The
Alliance combines key international markets through events such
as analytica Latin America, FCE Cosmetique, FCE Pharma, FOOD-
TECH & GLOBAL PACK and IPB China, thus creating powerful
synergies and a global range for exhibitors. Current topics from the
world of process engineering and the key sectors of industry are also
covered at the established POWTECH TECHNOPHARM Forum:
This is where companies have the opportunity to introduce themselves
and their innovative solutions to an interested public using
Stage Talks, and to engage in dialogue with the audience.
Once again in 2026, a further highlight of POWTECH TECHNO-
PHARM will be the special show by VDMA, a long-standing partner
to the exhibition: Current topics and solutions of interest will be displayed
under the heading “Clean Air – Smart Processing”, organized
by the two sector associations, Air Handling Technology as well
as Process Engineering Machinery and Apparatus, in collaboration
with their member companies.
Young, innovative companies from Germany will introduce themselves
at the sponsored “Young Innovators” joint stand again this year.
This area for start-ups will be complemented by an International
Start-up Area. Promoting new talents also remains a key component:
On the Student Day, POWTECH TECHNOPHARM invites educational
institutions and students to get to know the world of process
engineering in practice and make some valuable initial contacts.
Interaction and networking are also in focus at Women4Processing,
where dedicated women in industry, R&D, marketing and sales as
well as science gather to share knowledge, learn from each other and
create new inspirations for the process engineering industry. This
will be the second appearance for this networking format following
its launch at the previous edition of POWTECH TECHNOPHARM.
Virtual Talks, Industry Insights
– professional inspiration in the lead-up to the exhibition
Interested trade visitors will be able to gain extensive insights even
before the actual exhibition in September. POWTECH TECHNO-
PHARM offers a continuous programme online: In its VIRTUAL
TALKS webinar series, experts from the process engineering industry
regularly present solutions and applications on current industry
themes. Participation is free. And the Industry Insights platform offers
exclusive specialist presentations on developments, trends and
projects from the fields of chemicals, pharmaceuticals, food and other
process industries, including topics such as battery production,
containment, the circular economy, automation and digitalization. A
free monthly news service keeps subscribers up to date on an ongoing
basis.
NürnbergMesse GmbH
D 90471 Nürnberg
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photo © Netzer Group
Cleanroom with 100%
energy recovery from
the back process
© AdobeStock_1162820150
Florian Rusch, Head of the Energy Management Team at ÖLZ
the Master Baker, emphasizes: “Through an innovative process
to recover waste heat from our new toast and braided bread baking
lines, we make a substantial contribution to energetic circular
economy.” These measures are part of ÖLZ the Master Baker’s
comprehensive sustainability strategy, which also includes switching
to 100% renewable
electricity generated from
hydropower in Vorarlberg.
ÖLZ the Master Baker has set new standards in the production of
baked goods such as braided bread and toast in collaboration with
the internationally active engineering company NETZER GROUP
from Feldkirch (Vorarlberg, Austria).
As the general planner for building technology, NETZER GROUP,
specialized in cleanroom technology, took over the complete planning
of building services, including cleanroom facilities, and successfully
completed the implementation during ongoing operation
up to commissioning.
One of the central requirements was to recover almost all of the
energy generated during the baking process in terms of circular economy
and climate neutrality. With the expertise of NETZER GROUP,
this has been achieved. For ÖLZ the Master Baker, this means 100%
energy recovery from the baking process. This leads to a significant
reduction in gas usage and thus a reduction of approximately 245
tons of CO2 annually – an amount comparable to the gas consumption
of 141 households. Consequently, energy costs and CO2 emissions
for the company are significantly reduced.
Another milestone is the extension of the minimum shelf life without
preservatives. This is made possible because, prior to packaging,
residual heat and moisture that could promote mold growth
are vented out by specialized ventilation systems. Essentially, from
the oven through slicing to packaging, the products are protected
from mold spores under nearly sterile conditions, which extends the
shelf life of toast bread by up to two weeks. While other manufacturers
add alcohol to the dough, ÖLZ the Master Baker achieves this
through state-of-the-art cleanroom technology.
The planning and implementation of the project was a challenge,
especially coordinating the building services with the requirements
of the plant technology supplied by various companies across Europe.
Given the complexity and the multitude of technical infrastructures,
the NETZER GROUP project team opted for collaborative 3D
planning. This ensured a smooth construction process, adherence
to deadlines, and minimized additional costs, such as those caused
by modifications.
For large systems, efficient cost management is essential. This requires
knowledge of where and how it is feasible. NETZER GROUP has
this expertise. For example, the use of a certified BUS system to control
the mechanical smoke dilution system, which covers 19 smoke
zones and operates with six fans, resulted in a significant reduction
in procurement and maintenance costs.
The cooling is provided by machines using natural refrigerants,
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specifically ammonia (NH3 / R717). Due to its toxic and flammable
properties, strict safety regulations must be meticulously followed.
Despite the challenges posed by the COVID-19 pandemic, the project
was able to go into operation on schedule after 16 months of
construction, thanks to experienced planning, documentation, and
optimal communication with customers, suppliers, and contractors.
ÖLZ the Master Baker and NETZER GROUP are thus setting a new
standard in baking technology and sustainability.
NETZER GROUP GmbH
Studa 14
6800 Feldkirch
Österreich
Telefon: +43 5522 22818
eMail: info@netzergroup.at
Internet: http://www.netzergroup.at
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| www.cleanroom-online.com
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matched by none.
Fraunhofer FEP opens
biosafety level 2 laboratory
Behind this door, the future is being
explored: A look inside our biosafety level 2
laboratory. © Fraunhofer FEP, Finn Hoyer
The Fraunhofer Institute for Electron Beam and Plasma
Technology FEP has received regulatory approval to conduct
activities at biosafety level 2. The laboratory complex
thus opens up new research and testing opportunities for
industry and project partners. This approval marks an important
milestone in the development of the institute’s biomedical
laboratory unit.
With the construction of the RESET E building, Fraunhofer FEP
has laid the infrastructural foundation for innovative biomedical
and biotechnological research. The spacious laboratory complex
on the ground floor of the new building was occupied and put into
operation in the fall of 2023 by the “Biomedical Laboratory Unit”
working group. Following careful documentation and notification of
the planned activities, as well as an on-site inspection by the State
Directorate of Saxony, the competent authority granted approval in
November 2025. The laboratory is designed, both technically and
spatially, to meet all requirements for safe work with risk group 2 microorganisms.
Biological agents in this category can cause disease in
humans; however, their spread among the general population is considered
unlikely, and effective prevention or treatment is possible.
Safe technology for practical research
Biological safety level 2 significantly expands the Fraunhofer FEP’s
Safe disposal of biological materials: After the experiments
are completed, bacterial suspensions are safely inactivated
in an autoclave. © Fraunhofer FEP, Finn Hoyer
research scope. While the previous safety level 1 was limited to nonpathogenic
microorganisms, safety level 2 now enables safe work
with human samples, environmental samples, and moderately pathogenic
pathogens. For the institute and its partners, this represents
a direct gain in scientific and economic flexibility. The broader
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range of pathogens allows for research and testing opportunities that
are more relevant to real-world applications, enabling experiments
to be conducted under conditions that closely mimic real-world scenarios.
At the same time, the strict regulations of this containment
level lead to a significant increase in quality assurance and compliance
– a competitive advantage for customers and project partners.
The Biomedical Laboratory Unit conducts experimental work in
the fields of chemistry, biology, biotechnology, bioanalytics, and cell
biology. The projects are aligned with the strategic themes of Fraunhofer
FEP, including biotechnological resource extraction, sanitization,
tissue preparation, smart farming, and water and wastewater
treatment. In addition to applications for internal research projects,
customer- and project-specific experimental setups and protocols
are also implemented. Fraunhofer FEP’s unique strength lies in the
combination of technical expertise, modern technology, and strict
safety standards. Biological and chemical analyses are integrated
with the institute’s core competencies, with all sample preparation,
processing, and analysis conducted in-house. This enables reproducible,
legally compliant, and reliable results using state-of-the-art
methods and in accordance with current DIN standards.
New opportunities for innovative collaborations
“The approval of biosafety level 2 is the result of intensive, dedicated
work by all stakeholders involved,” says Marleen Dietze,
Biological Safety Officer at Fraunhofer FEP. “It opens up entirely
new possibilities for us to offer our customers and project partners
even more practical solutions. With this approval, we can address
research questions that were previously beyond our reach.
This significantly strengthens the competitiveness of the entire
institute.”
Looking ahead, Fraunhofer FEP plans to continuously expand
its service portfolio, extend the technology park, and build an expanded
collection of microorganisms and cells in order to open up
even broader application possibilities. In this regard, the laboratory
serves as a competent technology and service partner for both
industrial clients and public institutions. The institute is open to
diverse forms of cooperation and specifically targets stakeholders
in the fields of life sciences, environmental science, and biotechnology.
With the commissioning of the laboratory complex featuring
biosafety level 2, Fraunhofer FEP completes its infrastructure for
innovative research and services at the highest level. The institute
thus underscores its commitment to accompanying and supporting
companies and institutions in forward-looking developments.
Fraunhofer-Institut für Elektronenstrahl- und Plasmatechnik FEP
D 01277 Dresden
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Microfluidic chip:
The microfluidic chip: a diffusion bonded
manifold with precise channel structures.
Bioprinter for organs-on-a-chip:
The bioprinter prints living cells embedded in hydrogel
in tiny droplets directly onto the microfluidic chip.
Next-gen life science automation
Automation of organs-on-a-chip
for drug development
The development of drugs is lengthy, complex and expensive. Approaches from
organ-on-a-chip research promise to shorten the time to approval of new active
ingredients. Together with experts from TU Darmstadt, Festo has developed an
exhibit that demonstrates the automated production of such mini-organs: A bioprinter
applies human cell material to a microfluidic chip, on which organ-like
tissue then grows. Festo is combining two future technologies for the first time:
SupraMotion and Diffusion Bonded Manifolds.
The development of drugs takes a long time
and is very costly: a drug candidate first undergoes
several preclinical studies on cell
cultures or animals. Clinical trials on humans
follow in the final phase before authorisation.
In this phase, an average of five
drug candidates are tested per drug, four of
which fail in the end - so-called late fails.
The reason for this is that the results of preclinical
studies often do not translate well to
the human organism.
Much better results are achieved with
so-called organs-on-a-chip from the bioprinter,
on which efficacy and side effects
can already be tested more precisely in the
preclinical studies. Unsuitable candidates
are thus eliminated at a much earlier stage,
saving time and money. Organ-on-a-chip
(OoC) refers to microfabrication processes
that are used to create miniature models of
organs such as the heart, lungs or intestines.
Cells are arranged and cultivated on prefabricated
polymer or plastic carriers in such a
way that they form organ-like tissue.
Precise fluid control for
tissue engineering
Together with experts from TU Darmstadt,
Festo is demonstrating how the bioprinting
process can be automated - including
a solution for the contactless transport of
microfluidic chips equipped with bonded
manifold technology. Bonded manifolds are
multi-layered plastic manifold plates with
finely structured microchannels that enable
the precise dosing and handling of liquids.
SupraMotion: contactless working in
the laboratory of the future
Transport through the various steps in the
production process is carried out using
Festo‘s unique superconductor technology.
This allows objects to be transported contactlessly
on a magnetic levitator. The kinematic
system remains outside the clean
room and does not carry any particles away.
The surfaces are kept clean and are easy to
clean. The innovative technology can be
combined with automation solutions for the
life science sector to create a reliable overall
concept that fulfils the highest cleaning and
cleanliness requirements.
Diffusion Bonded Manifolds
from Festo: Nominated for the
Hermes Award 2026
Festo is among the three nominees for
the Hermes Award 2026 with its Dif-
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Automated production of organs-on-a-chip: Together with experts from
TU Darmstadt, Festo has developed a solution that demonstrates the
automated production of organs-on-a-chip. © Festo SE & Co. KG
SupraMotion transport System: Contactless transport with SupraMotion:
electric axes under the floor surface move the cryostat and the
magnetic carrier hovering above it from station to station.
fusion Bonded Manifolds. The Hermes
Award is one of the world‘s most prestigious
industry prizes and is presented at
the Hannover Messe for outstanding innovation
- products and solutions with a
particularly high degree of technological
innovation.
Festo as an automation partner
for life sciences
With flexible automation solutions, Festo
supports the transfer of innovative therapies
into clinical practice and makes state-ofthe-art
biotechnology available where it is
needed. With the help of its product portfolio
of pneumatics, electrics, software and
AI, Festo realises the perfect seamless automation
solution together with the customer.
Festo Vertrieb GmbH & Co. KG
D 73734 Esslingen
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Less CO2 emissions, no toxic chemicals:
Fraunhofer IPT develops a new process chain
for functionalized thin glass
The Fraunhofer Institute for Production Technology IPT
in Aachen, together with project partners, has developed a
process chain for manufacturing 3D thin glass with functionalized
surfaces. The process chain combines laser structuring
with subsequent forming and reduces energy consumption
as well as CO₂ emissions. The use of environmentally
hazardous etching chemicals is also no longer necessary.
Thin glass can be used in a variety of applications. It is especially
used where components need to be made thinner or of higher quality,
such as for high-end components in automotive or parts in electronics,
semiconductor industry, or sensor technology. In consumer
electronics alone, more than one billion components made from
thin glass are used annually, along with around 75 million units in
automotive manufacturing, sensor technology, and architecture. A
large proportion of these glasses feature intentionally added microand
nanostructures on their surfaces, for example for anti-reflective
coatings, controlling wettability, or for tactile feedback.
New process chain: First laser structuring, then forming
Currently, two main methods are used for surface structuring of thin
glass: In industrial practice, chemical structuring is the most common.
This method achieves good results but involves the use of environmentally
harmful etching agents, such as hydrofluoric acid. The
second method is replication through molding. Structures can also
be introduced into the glass surface at very high temperatures using
a mold tool while the glass is shaped into its final form. This method
also yields good results. However, the production costs, raw material,
and energy requirements are significantly too high to be economically
attractive and ecologically sustainable.
In the research project „EffF3D,“ the Fraunhofer IPT developed and
tested various process chains for the mass production of complexshaped,
functionalized thin glass. They consist of two steps: structuring
flat glass blanks with an ultrashort pulse laser (UKP laser) and
subsequent forming.
Laser structuring: High throughput using
polygon scanners and UKP laser
The structuring of flat glass blanks is performed with the UKP laser
and pulse durations of less than ten picoseconds. The low heat input
allows for particularly gentle processing of the material, enabling
the creation of micro- and nanostructures on glass that are effective
visually and tactilely.
The project team tested two complementary processing concepts.
In one, the laser beam is directed via two motor-driven mirrors.
These mirrors are continuously accelerated and decelerated,
which limits the processing speed. In the second method, the beam
is deflected by a very rapidly rotating mirror with many small facets.
Due to this continuous rotation, the laser can process large areas in a
very short time. With both configurations, the researchers were able
to produce anti-glare, anti-reflective, and anti-fingerprint structures.
Glass forming: comparison of different methods
To reshape the structured glass blanks, the researchers compared
two variants of hot forming: isothermal and non-isothermal forming.
In the isothermal process, the tool is heated together with the glass.
This method achieves particularly high dimensional accuracy but
has very long cycle times.
The non-isothermal process, developed at Fraunhofer IPT, se-
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parates the steps of heating, forming, and cooling. The glass
blank is first placed on a preheated forming tool and then
transferred into an oven. Due to its lower mass, the glass heats
up faster than the forming tool and is shaped accordingly.
Afterwards, the still hot glass is removed from the forming
tool and cooled outside the tool. The tool is then ready for
the next cycle. This approach allows cycle times of under 100
seconds per component.
Digital process monitoring and compensation
of structural distortions
In the „EffF3D“ project, various example components, including
functionalized center consoles and windshields, were
manufactured on series-like equipment. Since pre-structured
glass blanks were shaped for the first time in this way,
determining the optimal process temperature was a central
challenge: it must be high enough to enable forming but not
so high as to unintentionally affect the microstructures embedded
in the glass. The researchers used various sensors,
such as temperature sensors, for process monitoring.
The forming process alters the previously embedded
microstructures. To ensure that the structures end up with
the desired shape and position, the researchers developed
a compensation method that uses computer simulations to
predict the expected distortions in advance. These distortions
are taken into account during the structuring of the glass
blank, so that the correctly shaped structures are located at
the right position after forming.
Life Cycle Assessment demonstrates the potential
of the new process chain
As part of a Life Cycle Assessment (LCA), the process
chains were analyzed based on key ecological criteria such
as energy and material consumption. The analysis revealed
that the combination of laser structuring and non-isothermal
forming is very efficient regarding CO₂ emissions. Since
both processes—laser structuring and non-isothermal forming—are
fully electrically operated, their respective CO₂
emissions depend directly on the electricity mix used and
will continue to decrease with ongoing decarbonization.
Project partners
– Fraunhofer Institute for
Production Technology IPT (Coordination)
– Saint-Gobain Sekurit Deutschland GmbH, Herzogenrath
– FLABEG Automotive Germany GmbH, Nuremberg
– ModuleWorks GmbH, Aachen
– LPKF SolarQuipment GmbH, Suhl
– Vitrum Technologies GmbH, Aachen
Funding
The research project „EffF3D – Efficient Functionalization
of 3D Shaped Thin Glass“ was funded by the Federal Ministry
for Economic Affairs and Climate Action (BMWK) within
the framework of the 7th Energy Research Program of
the German government.
Fraunhofer-Institut für Produktionstechnologie IPT
D 52074 Aachen
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To estimate the force in the event of a collision, the robot strikes a force sensor, similar
to those used for measurement in cobots. © Fraunhofer IPA/Photo: Rainer Bez
Particle emissions are measured in a
cleanroom environment using a measuring
tube. © Fraunhofer IPA/Photo: Rainer Bez
Fraunhofer IPA develops
standardized analyses for
application-relevant criteria
of humanoid robots
To deploy humanoid robots in industrial applications, they must meet application-relevant
criteria. Fraunhofer IPA has developed a benchmark for this purpose.
This allows manufacturers and end users to have humanoid robots analyzied by
an independent third party for energy efficiency, cleanroom compatibility, data
security, and more.
The Fraunhofer Institute for Manufacturing
Engineering and Automation IPA has developed
a comprehensive benchmark for the
standardized analysis of humanoid robots.
For the first time, this allows manufacturers
and end users to have the actual capabilities,
safety, and operational suitability of these
robots objectively evaluated by an independent
third party. The modular benchmark
comprises six application-relevant criteria
and is based on internationally recognized
industry standards.
From media presence to
realistic assessment
Humanoid robots are omnipresent in the
media and fascinate with their human-like
appearance. Yet there is a vast gap between
spectacular presentations and actual capabilities.
“For end users and manufacturers
alike, it is essential to look behind the facade
sometimes constructed by marketing
agencies,” explains Simon Schmidt, Senior
Manager of the Business Unit Automated
Systems at Fraunhofer IPA. “The market is
too volatile and opaque to allow for a wellfounded
assessment and reliable evaluation
of humanoids for specific applications.”
What is the benchmark?
The Benchmark is a standardized service
in which research teams at Fraunhofer IPA
guide humanoid robots through various
challenges and scientifically evaluate the
results. The foundations for this were laid
thanks to funding from the Baden-Württemberg
Ministry of Economic Affairs, Labour,
and Tourism as part of the AI Innovation
Center “Learning Systems and Cognitive
Robotics.”
The modular structure enables manufacturers,
end users, and software providers
to specifically test the areas relevant to their
application. Where possible, the benchmarking
is based on established industry standards
that have been internationally recognized
for decades – for example, ISO 14644
for cleanroom suitability or ISO 10218 and
ISO TS 15066 for functional safety.
The benchmark is divided
into six key areas:
The tests and benchmarks are divided into six categories. © Fraunhofer IPA
1. Technologies and basic capabilities: Examination
of the installed sensors, AI models,
and gripper types, as well as tests of
walking speed, gripping forces, and manageable
loads. Objective measurements
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The ability to self-stabilize is examined through movements with different paths on a ramp. © Fraunhofer IPA/Photo: Rainer Bez
are recorded using a 3D tracking system
and force sensors.
2. Complex capabilities: Evaluation of practical
generic tasks such as stair climbing,
obstacle navigation, movement and force
precision, and reaction speed. The tests
are deliberately designed to be challenging
to ensure comparability with future
robot generations.
3. Cleanroom suitability: Evaluation of particle
emission according to ISO 14644-14,
outgassing behavior, and cleanability, all
critical for applications for example in the
semiconductor, pharmaceutical, or food
industries.
4. Functional safety: Central to human-robot
collaboration. Tests include stability
on various surfaces, force limitation during
collisions, obstacle detection, and
system behavior during failures. Collision
tests are conducted using the same force
sensors as those used for collaborative
industrial robots.
5. Cybersecurity: Four modules assess vulnerability
management, secure lifecycle,
network security, and penetration resistance.
These are important factors given
the increasing regulatory requirements.
6. Energy efficiency: Measurement of battery
life and power consumption in various
scenarios (standing, walking, walking uphill,
and walking with a load). The results
enable realistic deployment planning and
optimization of charging cycles.
Using the Unitree G1 as an example, Fraunhofer
IPA applied the benchmark comprehensively
for the first time. The technical
basis was the Unitree G1 EDU-4 with Dex3-1
3-finger hands delivered in May 2025 with
firmware version 1.04.
While the robot demonstrates good selfstabilization
and could be suitable for ISO
Class 5 cleanr ooms, significant limitations
also became apparent. In the event of collisions,
forces exceeding 500 newtons can
occur, what is far above the pain thresholds
permitted by the standard. In addition, the
researchers identified a critical Bluetooth
security vulnerability in the software at that
time that allowed attackers to take complete
remote control. This issue has since been
resolved. In terms of energy efficiency, the
maximum operating times on a single battery
charge were 2 hours and 49 minutes while
standing still and 1 hour and 49 minutes in a
typical scenario involving both standing and
walking.
Relevance of the Benchmark
for Companies
“Users can interpret the results directly and
thus find the right humanoid for the right
application,” emphasizes Werner Kraus,
head of the research division “Automation
and robotics” at Fraunhofer IPA. The benchmark
makes humanoids comparable not
only with each other but also with proven
automation components. This is particularly
important because:
– demographic change is forcing the use of
automation in areas previously handled
manually
– major investment decisions require wellfounded,
objective evaluation criteria
– safety standards for humanoids are not
expected until 2028 (ISO 25785-1)
– regulatory requirements for cybersecurity
are increasing
– sensitive production environments require
reliable data to prevent contamination
The benchmark provides transparency in an
opaque market and enables companies to
develop realistic expectations and minimize
risks.
Fraunhofer IPA plans to test additional
humanoids and establish a comparative
database. Manufacturers and users can now
commission individual benchmark modules
up to comprehensive evaluations and benefit
from the existing infrastructure and
expertise.
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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Focus on digital solutions for secure
and efficient communication
processes in pharmaceutical
production
New software company
Stormbit GmbH launched
(Image credit: Stormbit GmbH)
Hermann Schäfer
(Image credit: Stormbit GmbH)
With the foundation of the Stormbit GmbH,
the Systec & Solutions Group is expanding
its portfolio with a specialized software
company focused on data-driven production
environments and communication management.
Stormbit develops digital solutions
that integrate seamlessly into existing
systems and make production data available
in real time exactly where it is needed — directly
within the process.
The company’s portfolio includes context-based
visualization of production-relevant
data, device tracking solutions, and
continuous information availability throughout
the entire manufacturing process. In
addition, the application provides the foundation
for predictive maintenance concepts.
The goal is to improve transparency, efficiency,
and safety — particularly in regulated
industries such as pharmaceuticals, as well
as food and cosmetics manufacturing.
Many production environments still
face significant media discontinuities: despite
increasing digitalization, information
is often still documented on paper or distributed
across multiple systems. Especially in
sensitive areas such as GMP-compliant cleanrooms,
this can lead to deviations, delays,
and potential sources of error.
This is where Stormbit comes in. As a
spin-off of Systec & Solutions GmbH — an
internationally established specialist for
HMI systems in cleanroom environments
— the company combines deep process expertise
with modern software development.
Its mission: bringing data to where decisions
are made. Validated, in real time, and in the
right context.
“Providing the right information at the
right time in the right place is the key to
safe and efficient production processes,”
explains Hermann Schäfer. “In practice, however,
this information is often fragmented
or not digitized. With Stormbit, we close
this gap and deliver data exactly where it is
needed at the decisive moment. Stormbit
provides the technological foundation, by
integrating existing data sources and transforming
them into a seamless, actionable
view of processes and assets.”
VEYA: Paperless labeling and real-time
visualization in the cleanroom
One of the first examples is the VEYA
solution. The system enables paperless,
GMP-compliant labeling and visualization
of production-relevant data in cleanroom
environments. Through LCD-based HMIs,
ePaper-based labels (LSLs; Life Science Labels),
and a dedicated app, key information
such as production data, room parameters,
status messages, and cleaning states are displayed
in real time.
The data is sourced directly from existing
enterprise systems and centrally ma-
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naged, preventing conflicting or outdated
information — a common issue with manual
labeling processes. This significantly reduces
potential errors while also minimizing
manual documentation efforts through digital
data provisioning. The result is greater
transparency, improved process reliability,
and enhanced audit readiness.
Beyond data visualization, Stormbit’s
portfolio also includes additional scalable
applications that can be deployed across
industries — from pharmaceuticals to food
and cosmetics manufacturing.
Experienced Managing Director focused
on growth and international expansion
Stormbit GmbH is led by Hermann Schäfer,
an experienced entrepreneur with extensive
expertise in developing and scaling business
models.
Hermann Schäfer is an electrical engineer
specializing in communications
technology and combines technical expertise
with strong entrepreneurial execution
capabilities. Throughout his career, he has
successfully built and expanded numerous
companies — both organically and through
strategic partnerships and M&A activities.
Among his key achievements are the
establishment of a U.S. subsidiary and his
significant contribution to the growth of
Systec & Services, the predecessor company
of today’s Systec & Solutions GmbH,
culminating in its later acquisition by Körber
Pharma.
In additional leadership roles, including
as Business Unit Director at Possehl
Digital, Hermann Schäfer helped expand
an investment portfolio from three to ten
companies. His core strengths include
market expansion, scalable business model
development, and the successful implementation
of transformation and change
processes.
With a combination of technological
expertise, entrepreneurial experience, and a
strong focus on digital innovation, Hermann
Schäfer aims to strategically drive Stormbit’s
growth and position the company as a
strong partner for future-ready communication
solutions.
About Stormbit
Stormbit GmbH is part of the Systec & Solutions
Group and develops software solutions
for the context-based visualization
and utilization of production data. Its goal is
to make validated information digitally available
throughout the entire manufacturing
process — in real time, in the right place, and
without media discontinuities. In doing so,
Stormbit helps companies make processes
safer, more efficient, and more scalable.
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
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OHB CEO Marco Fuchs in the new cleanroom in Bristol
during the OHB Space UK celebrations. © OHB
At the signing ceremony for the ESA EnVision mission in
OHB Space UK’s new cleanroom: Dario Falleri (TAS),
Carole Mundell (ESA), Marco Fuchs (OHB),
Laura Costanza (ESA), Oliver Salisch (OHB),
Kim Lake (OHB), Kevin Guy (WECA),
Julie Black (UK Space Agency).
(From left to right) © OHB
Up to 100 new jobs planned in Bristol
– world class cleanroom facility under development
OHB Space UK: Growth, European
Cooperation and a Major Contract Win
The space and technology group OHB is celebrating the first anniversary
of its UK subsidiary OHB Space UK. Since expanding into
the United Kingdom in spring 2025, the Bristol site has developed
dynamically and has become an integral part of the Group’s international
growth strategy.
“Space is booming – and we are growing with it,” said Marco Fuchs,
CEO of OHB SE, during the anniversary celebrations in Bristol.
“With OHB Space UK, we are consistently pursuing our growth strategy
and sustainably strengthening Europe’s space capabilities. I am
very proud of the highly committed team in England and grateful for
the close and trusted cooperation with our partners in the United
Kingdom, Germany and across Europe.”
Starting from an initial team of around 14 employees, OHB Space UK
plans to grow to more than 100 highly skilled engineers within the
next five years. At the same time, one of the largest and most advanced
cleanroom facilities in England is currently being established at
the new Aztec West site in Bristol. In the future, institutional and
commercial satellites will be integrated and tested there. In addition,
OHB plans to develop state of the art space technologies at the Bristol
site and to build up system level capabilities.
A significant milestone in the company’s first year of operations is
its involvement in the European Space Agency’s science mission
EnVision. As part of the mission led by prime contractor Thales
Alenia Space, a joint venture between Thales (67%) and Leonardo
(33%), which is dedicated to the exploration of Venus, OHB Space
UK is responsible for assembly, integration and the comprehensive
test campaign of the EnVision spacecraft to qualify it for operation
in space. The multi‐million‐euro ESA project is being implemented
in partnership with Thales Alenia Space in Italy. During the anniversary
event, the participating parties signed a Preliminary Authorisation
to Proceed (PATP), formally initiating project activities at OHB
Space UK. The contract value is expected to amount to approximately
€24 million.
“OHB has firmly established itself as a valued and trusted partner
for ESA Science, and I am truly delighted to see the establishment
of OHB-UK, which further strengthens and showcases the UK’s industrial
capabilities. With the strong and complementary support
of TAS, I am fully confident that OHB-UK will rise to the exciting
challenge of integrating and testing the EnVision spacecraft and to
deliver outstanding results”, said Prof. Carole Mundell, Director of
Science at ESA.
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conditions suitable for life and contributing to the knowledge of the
formation and evolution of terrestrial planets.
© OHB
Envision is an ESA-led mission that will conduct a comprehensive
investigation of Venus, combining radar, spectrometers, and radio
science, to simultaneously sound its atmosphere, surface, and interior.
The holistic study of its exteriors, geological evolution and
internal dynamics will uncover how Venus evolved into a hostile
greenhouse world, while determining whether it ever possessed
UK Space Minister Liz Lloyd: “Signing this contract for a major role
in ESA’s EnVision mission to Venus is a clear signal that OHB Space
UK has already established itself as a trusted partner for world-class
missions. This is exactly the kind of high-value investment that will
drive the continued growth of our UK space sector.”
The signature event in Bristol took place in the presence of representatives
from politics, industry and the space sector. The guests
highlighted the positive development of OHB Space UK and welcomed
the company’s investment in the region. Bristol’s established
high-technology cluster provides a strong environment for the
development of competitive space products and systems. Helen
Godwin, Mayor of the West of England, said: “I am thrilled that OHB
Space UK are expanding and that the West of England will be making
a real contribution to such an important mission in space.”
One year after its establishment, it is clear that OHB Space UK is
here to stay – as a growing high-technology employer, a reliable industrial
partner for European space programmes, and a contributor
to a resilient and forward-looking European space sector.
OHB System AG
D 82234 Oberpfaffenhofen
Specialist doors
for the highest
cleanroom requirements
Contactless, hygienic and TÜV-certified – EFAFLEX highspeed
doors for the pharma industry are designed to meet
the stringent requirements of laboratories, pharmaceutical
production, medical technology, as well as the production
and handling of sterile packaging. The comprehensive range
of high-speed cleanroom doors provides tailored solutions
for a wide variety of applications. www.efaflex.com/pharma
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Ceremonial groundbreaking marks the start of the first construction phase
Vetter begins construction
of the new production site
in Saarlouis
– Pharmaceutical service provider celebrates groundbreaking with project partners
and representatives from land and region
– Production building with 50,000 m² area marks the start of construction work
– New location is part of global growth and investment initiatives
Vetter, one of the world‘s leading pharmaceutical service providers
for the aseptic manufacturing of injectable medicines, celebrates
the start of construction for the new site in Saarlouis with a traditional
groundbreaking ceremony. On the approximately 40-hectare
industrial site, a modern production facility for the commercial manufacturing
of injectable medicines will be built in the first phase.
Overall, Vetter will invest nearly half a billion euros at the site until
the planned commissioning in 2031. This underscores the company‘s
strong position as a technology leader with the highest quality
standards. Initially, 400 to 500 new jobs are planned. By the final
expansion stage of the first construction phase, the pharmaceutical
company expects up to 1,500 jobs. In the long term, up to 2,000 jobs
are possible.
The first expansion phase includes the construction of a 50,000 m²
production building as well as other production-related facilities
such as laboratories and warehouses. Initially, three state-of-the-art
cleanrooms are planned for the aseptic manufacturing of innovative
and complex medicines – two cleanrooms for filling pre-sterilized
syringes and one cleanroom for filling vials.
Representatives of the pharmaceutical service provider Vetter, the economic development agency gwSaar, as well as political representatives
from the city, district, and state at the symbolic groundbreaking ceremony for the new production site in Saarlouis (from left to right):
Nicholas H. Vetter, Thomas Schuck, Henryk Badack, Jürgen Barke, Gunther Strothe, Anke Rehlinger, Honorary Senator Udo J. Vetter,
Marc Speicher, Patrik Lauer, Wolfgang Kerkhoff. © Vetter Pharma International GmbH
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Voices on the groundbreaking ceremony
Senator h.c. Udo J. Vetter, Chairman of the Supervisory Board and
member of the family ownership: “The groundbreaking today marks
a decisive step for the future of our family business. With the new
site in Saarlouis, we are setting the course for further sustainable
growth. We are creating the prerequisites to further expand our capacities
in the manufacturing of complex medicines and to continue
providing our international customers with the resources, quality,
and reliability they need and expect from us. At the same time, we
are sustainably strengthening the industrial location Germany.”
Anke Rehlinger, Prime Minister of Saarland: “Today is a good day for
Saarland: With Vetter, a strong, innovative company is coming to us –
and with it, new opportunities for many people. Here in Saarlouis, it
shows: structural change succeeds when we actively shape it.”
Jürgen Barke, Minister of Economics of Saarland: “Such a high-tech
settlement makes us one of the most desirable locations for the
pharmaceutical industry and shows how transformation succeeds:
new, sustainable jobs and a strong future industry. This will trigger
ripple effects like we have not seen before.”
Patrik Lauer, District Administrator of Saarlouis: “Together with
Vetter as an anchor, we want to usher in a new economic era in our
region and write another success story. We look forward to a strong
company that, with its innovative strength, will attract other businesses
from nearby industries. We are ready for this with a well-trained
and motivated workforce, an excellent educational offering, and
an outstanding infrastructure.”
Marc Speicher, Mayor of Saarlouis: “The settlement of Vetter strengthens
the economic location of Saarlouis and Saarland. As a successful,
international family business, Vetter fits perfectly with our Saarlouis
economic and settlement strategy. Vetter is not only investing
here with us in Saarlouis, but we are also entering into a long-term
community and development partnership: for a strong economy and
good jobs. We processed the settlement at the town hall in record
time, and I look forward to the years ahead with Vetter in Saarlouis.”
Global investments in the future
For over 75 years, Vetter has stood for quality, innovation, and responsibility
to improve the quality of life for patients worldwide. To
meet the growing demand and increasing market requirements, the
company is sustainably investing in its pharmaceutical production
sites in Germany, Austria, and the USA. With the new site in Saarlouis,
Vetter is significantly expanding its production capacities
once again.
Vetter Pharma International GmbH
D 88212 Ravensburg
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Expansion of capacities for strategic products PURELAY® and VISTAFORM®
Etimex Primary Packaging
invests in the future
of the Dietenheim site
The ETIMEX Primary Packaging GmbH based
in Dietenheim continues to expand its
production capacities and invests strategically
in the future of the site. The current
investment focuses on increasing capacity
for the strategic product lines PURELAY®
and VISTAFORM®. Additionally, a new cleanroom
area of class 7 is being created. The
completion of the project is planned for the
first quarter of 2027.
With this investment, the company responds
to the increasing demand for innovative
and sustainable packaging solutions
for the pharmaceutical industry and simultaneously
emphasizes its long-term commitment
to the Dietenheim location.
The pharmaceutical industry is currently
undergoing a fundamental transformation.
Increasingly, sustainable materials, recyclability,
and resource-efficient packaging
solutions are coming into focus. Traditional
blister packs based on PVC/aluminum are
increasingly criticized because they are not
recyclable. Modern monomaterial solutions
offer a future-proof alternative, as they enable
significantly better recyclability while
meeting the highest requirements for product
protection and process security.
Cleanroom production according
to ISO 15378 and GMP
As part of the expansion, ETIMEX is also
building new cleanroom capacities designed
according to the international standard
ISO 15378. This standard combines the requirements
of „Good Manufacturing Practice“
(GMP) with a certified quality management
system for primary packaging materials
of pharmaceuticals.
For manufacturers of pharmaceutical packaging,
this means particularly strict requirements
for the production environment,
process control, traceability, and quality assurance.
The goal is to minimize the risk of
contamination and ensure consistently high
product quality.
The new cleanroom area enables ETIMEX
to produce sensitive pharmaceutical applications
under controlled conditions and to
optimally meet the increasing regulatory
requirements of the industry. At the same
time, the company creates additional capacities
for future growth in strategic product
segments.
PURELAY® – The original PP
monoblock blister since 1989
PURELAY® is considered the original
among polypropylene monoblock blister solutions.
The innovative and award-winning
packaging technology is based on a fully polypropylene
composite material, enabling a
true monomaterial solution for pharmaceutical
blister packs.
Groundbreaking in Dietenheim – in the picture, from left to right:
Christoph Eh (Mayor of Dietenheim), Martin Rank (Head of Marketing & Sales),
Manuel Strauch (Plant Manager), and Rainer Gebken (Managing Director)
By using PURELAY®, pharmaceutical
companies can significantly reduce material
usage, improve the recyclability of their
packaging, and thus also their carbon footprint.
The material meets the highest requirements
for barrier properties, stability, and
processability in existing packaging lines.
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Additionally, PURELAY® offers excellent
transparency and high mechanical durability
– important properties for the safe protection
of sensitive pharmaceutical products.
„PURELAY® has been the original PP monoblock
blister solution since its introduction
by ETIMEX Primary Packaging (then
BP Chemicals) in 1990. In our nearly 40 years
of experience, ETIMEX has developed
the former pioneering achievement into a
widely proven and mature product. With
our current investment, we are specifically
strengthening the capacities for this forward-looking
product and actively supporting
our customers in the transition to more
sustainable packaging solutions,“
VISTAFORM® – PP thermoforming
films for modern food packaging
In addition to PURELAY®, ETIMEX is
also investing in expanding capacities for
the VISTAFORM® product line. These are
high-quality polypropylene thermoforming
films for the food industry.
The VISTAFORM® films are available both
with and without an integrated oxygen barrier.
In barrier variants, ethylene-vinyl alcohol
(EVOH) is used, which provides an effective
oxygen barrier and thus helps extend
the shelf life of sensitive foods.
The thermoforming films are suitable for a
variety of applications, including packaging
for sausage and dairy products, convenience
foods, snacks, as well as vegetarian and
vegan products. Due to their excellent thermoformability,
they enable stable and precise
processing on modern packaging lines.
Strategic investment
in the Dietenheim site
The investment in expanding production
capacities is also a clear commitment to the
Dietenheim location. ETIMEX is thereby
further strengthening its role as an important
industrial employer and innovation hub
in the region.
„The expansion of production capacities
clearly shows that ETIMEX is investing
long-term in the Dietenheim site and shaping
the future here. The company is an
important employer and innovation driver
for our region. We expressly welcome this
investment,“
Our investment is a clear signal of the future
viability of our location. Dietenheim is the
heart of our production and a central component
of our innovation strategy. With the
expansion of our capacities and the new cleanroom
structures, we create the conditions
to continue growing as a reliable partner for
the pharmaceutical and food industries in
the future,“
ETIMEX Primary Packaging GmbH
D 89165 Dietenheim
BioCapt® Single-Use Microbial Air Sampler
for a Continuous Cleanroom Monitoring
Learn more
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(Sartorius Freiburg)
Sartorius opens new
competence center for cell
and gene therapy components
in Freiburg
– Production capacity of quality-critical materials for the
dynamic cell and gene therapy market in Freiburg more than doubled
– Opening in the Haid industrial park with around 180 guests
– Investment amount of more than 140 million euros
– Future-proof building technology: no use of fossil fuels
geothermal energy provides heat, well water
for cooling, and photovoltaic systems for
electricity generation. The construction has
already been awarded the Gold pre-certification
by the German Sustainable Building
Council (DGNB) for its consistent focus on
sustainability.
„The expansion of the site is the result of
very close and constructive collaboration
over many years. We would like to especially
highlight the support of the city of Freiburg
as well as the involved planning, construction,
and technology partners. Together, a
place has been created here that combines
cutting-edge research and production
technology with sustainability,“ said Daniel
Spatz, Managing Director of Sartorius Cell-
Genix in Freiburg.
The life sciences company Sartorius has
opened a new competence center in Freiburg
im Breisgau for the development and
production of quality-critical materials for
the cell and gene therapy market. In Freiburg,
the company produces essential
components such as cytokines or growth
factors used in innovative therapies. With
an investment of more than 140 million euros,
Sartorius affirms its strategic focus on
the emerging business field: cell and gene
therapies are gaining significant global importance
and already account for around 30
percent of the development pipelines for
medicines today.
„Cell and gene therapies give patients
worldwide hope for cures for diseases that
were previously considered untreatable. Cytokines,
growth factors, and cell culture media
are crucial for the development and manufacturing
of these innovative therapies.
The Freiburg site is an important part of our
global network for these critical materials
and this dynamic market, which demands
high speed, scalability, and process safety.
With the significantly expanded capacities,
we can respond much more flexibly to the
demands of our biopharma customers and
support them even better in bringing cell
and gene therapies to patients faster and
more efficiently,“ said René Fáber, Head
of the Bioprocess Solutions division and
member of Sartorius‘ Executive Board.
In the Haid industrial park, state-of-the-art
production, laboratory, and office spaces
have been created on approximately 18,000
square meters for up to 180 employees. The
new building meets the highest GMP quality
standards and thus strict requirements
of the biopharmaceutical industry. Additionally,
due to innovative building technology,
it operates entirely without fossil fuels:
The opening of the new plant marks an important
milestone in the development of
the Freiburg site: In 2021, Sartorius acquired
the majority of CellGenix GmbH, founded
in 1994 at the University Hospital Freiburg;
since early 2026, the company has been fully
integrated into the Sartorius Group. Over
the past five years, the number of employees
in Freiburg has nearly doubled to around 140
people.
The site expansion in Freiburg is part of a
long-term investment program to expand
Sartorius‘ global development and manufacturing
network. The goal is to prepare the
company for further organic growth, strengthen
its resilience, and continue to ensure
high delivery reliability and consistent product
quality across all locations.
Sartorius AG
D 37079 Göttingen
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In Fehring, AT&S invests in
key technologies of the future
The Styrian high-tech company is strengthening its plant in Fehring with a comprehensive
investment program. More than EUR 30 million will be invested in
new technologies, sustainability and additional jobs. 50 new jobs and an apprentice
workshop for skilled worker training will be created.
strong commitment to the plant, the region
and the expertise of our team. The positive
development shows that with our strategy
and clear customer focus, we are on the right
track,” adds AT&S CEO Michael Mertin.
In addition to major investments at its headquarters
in Leoben, AT&S is also consistently
advancing the strategic development of its
plant in Fehring. Following a phase of consolidation,
the company is making targeted
investments in future oriented business
areas and further expanding its technological
expertise. The focus in Fehring is on applications
in e-mobility, semiconductor test
equipment as well as in the fields of medical
technology, aerospace and defense.
Significant investments in
key technologies of the future
Funds will be allocated to specific future
projects in Fehring through March 2027:
around EUR 8.8 million will be invested in
production for semiconductor test equipment.
A further approximately EUR 10
million relates to a strategic project for innovative
inverter solutions in the field of
e-mobility, in which AT&S acts as the sole
supplier for a German premium manufacturer.
In addition, around EUR 7 million will
be invested in new production technologies
for technologically demanding applications.
Approximately EUR 4 million will be used to
implement sustainability measures, including
renewable energy, recycling concepts
and sustainable heat supply as part of the
“Raus aus Gas” project. Over the past two
financial years, AT&S has already invested
EUR 16.5 million in the plant, with a further
EUR 14 million planned.
AT&S continues its upward trend
“We have repositioned ourselves and are
investing specifically in technologies with
strong future relevance. Around 70 percent
of the funds are being directed into innovative
products that are strategically important
for our customers,” says Christopher Hermann,
Director Operations and Plant Manager
in Fehring. “These investments are a
The investment program is also accompanied
by workforce growth. 35 additional employees
have already been hired and a total
of around 50 new positions are planned. An
in-house apprentice workshop is also scheduled
for 2026 to ensure the sustainable
development of skilled workers. With this
expansion step, AT&S underlines the strategic
importance of the Fehring plant and
strengthens the company’s long-term competitiveness
in Europe.
Measured by revenue, AT&S Fehring is one
of the largest printed circuit board plants in
Europe and is increasingly benefiting from
rising demand for security relevant hightech
solutions produced in Europe. With its
own engineering department, the plant is
also enhancing its ability to independently
develop new printed circuit board technologies.
AT & S Austria Technologie & Systemtechnik
Aktiengesellschaft
AT 8700 Leoben
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Permanent clearly readable black marking („Black Marking“),
labeled with the FOBA F.0100-ir ultrashort pulse laser.
(Copyright: FOBA)
Stainless steel instrument with „Black Marking“.
The marking was done using the ultra-short pulse laser
FOBA F.0100-ir. (Copyright: FOBA Laser Marking + Engraving)
Shiny metals, extremely small marking areas, and strict UDI requirements pose challenges
for direct marking of medical devices. The technical article shows how ultrashort pulse
lasers solve these through the marking effect „Black Marking.“
More contrast, less risk:
„Black Marking“ for medical technology
With UDI requirements according to FDA and MDR, direct marking is mandatory
for many medical devices, including surgical instruments and implants. In
practice, these requirements apply to highly reflective metals, extremely limited
marking areas, and demanding conditions throughout the entire lifecycle. Markings
must be permanently contrast-rich and reliably legible without impairing
function or material properties. Black marking with ultrashort pulse lasers, also
called “Black Marking,” has established itself as a reliable solution for these challenges.
It is especially preferred on medical stainless steel, but it is also suitable
for other metals.
Four hurdles in direct marking
of medical stainless steel
Stainless steel is indispensable in medical
technology due to its corrosion resistance,
mechanical stability, and biocompatibility.
Direct marking of medical stainless steel is
technically demanding. Four points should
be particularly considered:
1. Reflections on polished surfaces
High-gloss surfaces complicate direct marking,
optical inspection, and code verification.
Reflections reduce readability.
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2. Very small marking fields
and complex geometries
On micro-instruments or functional surfaces,
often only minimal space is available.
Codes must be extremely fine, precise, and
simultaneously reliably legible.
3. Thermal influences and
risk of corrosion
Thermally induced marking processes can
affect passive layers and surface properties.
The balance between contrast, corrosion
resistance, and material integrity must be
considered.
4. Stress from processing
Cleaning, disinfection, sterilization, and
possibly passivation repeatedly affect the
surface. Markings must remain durable and
corrosion-free during these processes.
The combination of reflection, miniaturization,
material sensitivity, and processing
stress means that classical laser marking
methods (e.g., material removal or annealing
marking) reach their limits for certain marking
requirements. Precisely at this point,
“Black Marking” demonstrates its strengths,
as it can address all four challenges simultaneously.
Working principle of “Black Marking”:
Nanostructure instead of heat input
“Black Marking” refers to a laser marking
effect that produces deep black, matte, and
non-reflective markings. It is characterized
by angle- and light-independent readability:
The inscription appears uniformly black regardless
of viewing angle and lighting. This
is especially relevant for camera-based inspection
processes and the reliable machine
readability of DataMatrix codes, which
are common in UDI marking.
“The black marking is created not by material
removal or thermally generated oxide
layers, but by a nanostructure on the surface.
These so-called ‘light traps’ reduce reflection,
resulting in a strong contrast,” explains
Damian Zawadzki, Product & Application
Manager at FOBA Laser Marking + Engraving.
Ultrashort pulse lasers are used for the
“Black Marking” process. The ultrashort pulses
in the femto- and picosecond range with
high pulse energy create the nanostructures
necessary for the “Black” effect practically
without heat input. Because the pulse duration
is so short, little energy is transferred to
the surrounding material, often described as
“cold laser marking.”
NEWSLETTER | Ausgabe EN 07-2026
Long-term tests by medical technology service
provider add’n solutions and FOBA Laser
Marking + Engraving demonstrate that
durability can also be proven under realistic
conditions: Stainless steel instruments marked
with the “Black Marking” process were
repeatedly processed (cleaned/passivated
in fully automated systems, autoclaved, and
subjected to additional highly alkaline cleaning
intervals). The test results: After 1,000
cycles, the markings produced with the ultrashort
pulse laser FOBA F.0100‘ remained
reliably legible. “The marking is still highly
readable. It endures the lifespan of an instrument.
The material of the test instruments
failed before the marking did,” reports Dominik
Pfeiffer from add’n solutions.
Regarding the four challenges mentioned
above, the summary is: “Black Marking” with
ultrashort pulse lasers combines reflectionfree
contrast creation, high precision for
miniaturized codes, extremely minimized
heat input to protect the material, and high
durability against cleaning, disinfection, and
sterilization processes.
“Black Marking” in practice: Application
examples
1. Permanently readable UDI codes
on highly polished stainless steel
instruments
Initial situation: A manufacturer of surgical
instruments needed a permanently durable,
corrosion-free UDI marking on a highly
polished stainless steel surface. Classic
marking methods with fiber lasers provided
insufficient contrast or caused surface
changes. Additionally, reflections hindered
machine readability. Standard ultrashort
pulse lasers also did not meet the customer’s
expectations.
Solution: The decisive factor for a secure
marking was the infinitely adjustable pulse
width of the FOBA F.010‘ ultrashort pulse
laser: This allows highly precise and optimal
adjustment of the energy input to the material
and surface condition. As a result, a deep
black, reflection-free contrast is created
without affecting the material or function.
Added value: Permanently stable, processsafe,
and corrosion-free marking of reliably
readable UDI codes — even after countless
cleaning and sterilization cycles.
2. Reliable readability of miniaturized
codes on dental implants
Initial situation: A manufacturer of dental
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Ultrashort pulse laser from FOBA with continuously adjustable pulse width and laser-integrated camera system. (Copyright: FOBA)
implants faced the challenge of reliably marking
very small fields with high information
density. The shiny surfaces complicated machine
readability, and the marking had to be
precisely positioned on the small area.
Solution: The high precision of the FOBA
F.0100‘ ultrashort pulse laser and the laserintegrated
vision system IMP (Intelligent
Marking Positioning), combined with the
MarkUS software, were crucial for solving
this challenge. By optimally adjusting all parameters,
the laser enables delicate “Black”
marking structures on the smallest surface.
The non-reflective, deep black marking
is reliably machine-readable. The FOBA
workflow, based on software and vision,
ensures exact, automated positioning and
code verification.
Added value: Reliable readability even of
the smallest codes, minimized scrap rate
through high-precision positioning, and a
stable marking process.
Practical tips for process design and
quality assurance in “Black Marking”
In regulated environments, not only the
quality of the marking is crucial. Equally important
for the safe labeling of medical devices
is that the entire marking process is stable
and qualified. The following points have
proven effective in practice for successful
“Black Marking”:
1. Consider material and surface early
Alloy, surface finish, and cleanliness signi-
ficantly influence the parameter range in
which a stable contrast is achieved. Even
minor changes in the material or surface
preparation can shift the process window.
Laser expert Damian Zawadzki recommends:
“When conducting marking tests,
always consider the actual serial condition
of the components.”
2. Adjust parameters specifically
to material and application
A reliable “Black” marking process requires
precise adjustment of laser parameters such
as pulse energy, pulse duration, repetition
rate, and focus position. Testing on original
parts is the safest way to achieve reliable results.
“Our application laboratories conduct
multiple tests with different settings. This
way, we determine the optimal parameters
that meet customer requirements,” reports
Zawadzki.
3. Include downstream processes
The product lifecycle (e.g., cleaning, sterilization,
or passivation) should be part of process
qualification and considered from the
beginning to ensure marking security.
4. Consider inline inspection
and documentation
Especially for UDI applications, direct
verification of code quality after marking
using an integrated vision system is
recommended. Camera-based inline inspections
reduce early risks, while software-recorded
process data support auditability
and traceability.
5. Mark, verify, and document
as an integrated system
Maximum safety and stability are achieved
when the entire marking process is viewed
holistically. This means considering
all steps—from component positioning to
documentation. A closed marking process,
such as FOBA’s workflow, reduces interfaces,
simplifies validation, and maximizes
stability. FOBA combines laser technology,
software control, automated marking alignment,
vision inspection, and documentation
into a coordinated overall system.
“Black Marking”: Technology
and process at a glance
“Black Marking” with ultrashort pulse lasers
offers a technically convincing solution for
the demanding direct marking of metallic
medical devices. The deep black, reflection-free
contrast, high durability against
cleaning and processing, and the nearly
heat-free marking process address central
challenges in medical device labeling.
However, the key to sustainable success is
not only the marking effect but also a wellthought-out
overall solution: only a stable,
qualified workflow ensures that markings
meet long-term regulatory, functional, and
safety requirements.
FOBA Laser Marking + Engraving
D 23923 Selmsdorf
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Northern Europe‘s leading 3D printing provider
opens location in Dornbirn
Expansion: Prototal Group
launches service for
rapid series production
in the DACH region
Prototal Group is now also manufacturing series components made of plastic
in the DACH region. Northern Europe‘s largest provider for industrial 3D
printing and injection molding has opened a location at the headquarters of
its specialized subsidiary 1zu1scale in Dornbirn. With its own sales structure
and integration into the production network, Prototal Group enables flexible
series production with secure supply chains in the DACH region. The offering
is primarily aimed at companies in aerospace, defense, and the automotive
industry.
With over 130 industrial 3D printing systems,
more than 110 injection molding machines, integrated
toolmaking, and 10 production sites,
Prototal Group is one of Europe‘s leading providers.
The corporate group, headquartered in
Jönköping (Sweden), covers the entire value
chain from prototype to series production. Prototal
Group is a production partner for various
industries and operates specialized competence
centers for aerospace, defense, and the automotive
industry.
The newly founded subsidiary Prototal GmbH
in Dornbirn provides customers in the DACH
region with direct access to the European production
network. They now benefit from flexible
manufacturing, technological diversity, and the
group‘s extensive material portfolio. „Trust is
the key to successfully scaling new product solutions
globally. This requires good service and,
above all, local consulting,“ emphasizes Jan Löfving,
CEO of Prototal Group. The geographically
favorable location in the Lake Constance region
is easily accessible for customers from Germany,
Austria, and Switzerland.
Digital supply chain for operational resilience
Prototal Group starts in the DACH region: Northern Europe‘s largest provider
for industrial 3D printing operates more than 130 machines. (Photo: Prototal Group)
The decentralized network offers high capacities
and provides security and stability. „As a
strategic partner, we reliably protect our customers‘
series production from disruptions.
Production processes remain predictable even
under demanding market conditions,“ says
Business Developer Kilian Rottenberger. Risk
minimization is also achieved thanks to the digital
supply chain. Prototal Group manufactures
components and spare parts on demand. The
„cloud warehouse“ reduces physical inventory
costs and shortens downtime from months to
days.
Global expansion strategy
Prototal Group is expanding and now also offers
fast serial production with 3D printing for customers
in the DACH region. (Photo: Prototal Group)
Kilian Rottenberger is
responsible as a Business
Developer at Prototal GmbH
for clients in the DACH region.
(Photo: Prototal Group)
Prototal Group‘s market entry into the DACH
region is part of its worldwide growth strategy.
Over the past few years, the group has built global
sales structures for industries such as aerospace,
defense, and mobility, and has invested in
new machinery at all locations. „Through Prototal
Group, we offer innovative companies direct
access to Europe‘s leading network for additive
manufacturing and plastic injection molding.
For small, delicate components with high requirements
such as ISO 13485 certification or
cleanroom environments, 1zu1scale is the right
address,“ explains Jimmy Müller, Head of Sales
at Prototal GmbH.
Prototal Group
SE 553 02 Jönköping
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The most advanced lithography system, crucial for
future advanced memory and computer chips,
will play a key role in scaling up quantum technology.
Functioning array of qubits with gaps between
plunger (P) and barrier (B) gates of barely
6 nanometers, enabled by High NA EUV
lithography. The image also shows the
accumulation gates (A) and confinement (C).
World first: imec presents quantum dot qubit
device using High NA EUV lithography
1. Imec presents a world first: a quantum dot qubit device fabricated
using High NA EUV lithography.
2. This demonstration marks a milestone toward the industrial scaling of
more reliable qubits, the basic computational units of quantum computers.
Quantum computers will perform exponentially better in specific
computational challenges, such as developing new drugs or simulating
physical processes.
3. By building on a base layer of precise patterns using High NA’s precision,
imec has succeeded in fabricating a functioning network of qubits with gaps
of barely 6 nanometers. Thanks to the nanoscale of this hardware component,
millions of quantum bits can theoretically be integrated onto a single chip.
4. “We can leverage decades of semiconductor innovation and reuse the entire
ecosystem of silicon scaling, moving quantum devices beyond lab experiments
to large-scale, manufacturable systems. This is where silicon-based
qubits have a clear advantage”, explains Sofie Beyne, project leader and
quantum integration engineer at imec.
At ITF World, imec, a world-leading research
and innovation hub in advanced
semiconductor technologies, presented a
world first: a quantum dot qubit device fabricated
using High NA EUV lithography.
This achievement marks a milestone toward
the industrial scaling of more reliable qubits,
the basic computational units of quantum
computers. To the best of our knowledge,
this is the first integrated hardware device
created using High NA EUV lithography.
For specific, complex computational problems,
such as developing new drugs or
simulating physical processes, a quantum
computer could perform exponentially better
than classical computers. However, for a
useful quantum computer, we need to scale
to millions of connected qubits (the computational
units of a quantum computer), with
high reliability and precise control.
Of the various quantum platforms currently
under investigation, silicon quantum dot
spin qubits are considered a promising candidate
for industrial scaling and are often
referred to as ‘the industry qubits’. Their
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production process is largely compatible
with the production of standard computer
chips on silicon (CMOS), a research domain
in which imec has built global authority over
the past decades.
“We can leverage decades of semiconductor
innovation and reuse the entire ecosystem
of silicon scaling, moving quantum devices
beyond lab experiments to large-scale, manufacturable
systems. This is where siliconbased
qubits have a clear advantage”, Sofie
Beyne, project leader and quantum integration
engineer at imec, explains.
Silicon quantum dot spin qubits confine an
electron within a silicon nanostructure (the
gate layer). The ‘spin state’ of the trapped
electron is used to store quantum information.
Gaps between the various gates must
be minimized to limit environmental noise.
Imec has succeeded in fabricating a functioning
network of qubits with gaps of barely
6 nanometers. Thanks to the nanoscale
of this hardware component, millions of
quantum bits can theoretically be integrated
onto a single chip.
“High NA EUV enables the precise patterning
of silicon quantum dot qubits. As the
coupling strength between neighboring
quantum dots increases exponentially with
the gap between them, we need to reliably
pattern gaps of a few nanometers between
the control electrodes of the quantum dots.
This is a true engineering feat, thanks to
our integration and patterning teams and
ASML‘s outstanding high NA EUV technology”,
says Kristiaan De Greve, imec fellow
and program director Quantum Computing.
This demonstration builds on imec’s previous
results with silicon quantum dot spin
qubits, which already demonstrated that
CMOS-compatible processes can lead to
low charge noise and stable qubit operation.
By adding High NA EUV lithography to the
production process, the focus shifts from
individual demonstration devices in the lab
to 300mm fab-compatible, reproducible
quantum bits.
While it’s obvious that High NA EUV lithography
will be crucial for sub-2nm logic
and high-density memory technologies
that fuel the rapid growth of advanced AI
and high-performance computing, it is now
becoming clear that it will also play a pivotal
role in hardware for future quantum computing.
IMEC Belgium
BL 3001 Leuven
Dominic Böhm as of now Head of Sales
Thermoplast Germany
SHIBAURA MACHINE LWB GmbH is strengthening its sales team. Dominic
Böhm is taking on the position of Head of Sales Thermoplast Germany effective
immediately. With over 20 years of experience in injection molding technology,
plastics processing, and automation, he will practically support customers with
demanding applications in injection molding production.
Practical experience along the entire process
chain of injection molding production
“Dominic Böhm brings comprehensive
know-how in plastics processing as a
trained process mechanic and technician
for plastics and rubber technology. He
will practically assist plastics processors
Dominic Böhm, effective immediately,
Head of Sales Thermoplas Germany
at SHIBAURA MACHINE LWB GmbH.
and injection molders in Germany to optimize
their production processes, produce
high-quality end products, and plan,
implement, and commission automated
production cells,” says Dr. Georg Holzinger,
Managing Executive Officer of SHI-
BAURA MACHINE and spokesperson for
the management of SHIBAURA MACHI-
NE LWB GmbH.
Dominic Böhm began his professional
career in manufacturing technology in the
automotive supplier industry. There, he was
responsible for the design and project planning
of complex injection molding systems.
He accompanied the commissioning of tools
and optimized production processes in projects
across Europe, India, China, and Mexico.
During this time, he gained practical
experience with solutions from SHIBAURA
MACHINE and LWB, including projects in
India and Spain. Most recently, Böhm led
application technology at a manufacturer of
injection molding machines and supported
technology-intensive customer projects.
“I have been working closely with production
in the injection molding industry
for 20 years. SHIBAURA MACHINE LWB
stands for outstanding competence in injection
molding technology and automation.
My goal is to practically help plastics processors
and injection molders in Germany
achieve the highest efficiency, precision,
and reliability,” says Dominic Böhm. He reports
to Dr. Martin Kovacik, Executive Vice
President of Thermoplast Sales and Service
EMEA.
At the Kuteno in Bad Salzuflen from
June 9 to 11, Stand 20-E43, SHIBAURA
MACHINE LWB, the German subsidiary of
the Japanese machine manufacturer SHI-
BAURA MACHINE, will inform plastics
processors and injection molders about the
advantages of its broad portfolio. This includes
vertical and horizontal fully electric
injection molding machines with clamping
forces up to 3,000 tons, as well as automation
solutions for processing thermoplastics,
elastomers, and silicone.
Shibaura Machine LWB GmbH
D 84032 Altdorf
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Modular Software Platform for Pharma 4.0: Virtual Planning and Certifiable Quality
Fraunhofer IESE Develops VIMOPROP
for Digital Pharmaceutical Production
The Fraunhofer Institute for Experimental Software Engineering IESE has developed
VIMOPROP, a modular software platform that supports pharmaceutical
manufacturers in the virtual design, simulation, and commissioning of production
processes. The platform makes a concrete contribution to the implementation
of Pharma 4.0 by combining digital twins, modular production concepts, and
integrated quality assurance in a consistent digital approach. The goal is to make
complex production environments – particularly for the manufacture of Advanced
Therapy Medicinal Products (ATMPs) – more flexible, efficient, and compliant
with regulatory requirements.
Virtual planning and modular
production design for Industry
With VIMOPROP, production facilities can
be assembled from pre-planned, reusable
modules with plug-and-produce capabilities.
Digital twins and simulations realistically
model plant components and processes,
enabling virtual testing, scenario comparisons,
and informed decisions regarding
process planning or adaptation, product
changes, and scaling – while significantly
reducing the need for physical trials.
“The pharmaceutical industry faces the
challenge of designing highly complex processes
in a flexible manner while simultaneously
meeting the strictest regulatory
requirements. With VIMOPROP, we have
created a digital foundation to systematically
ensure quality and regulatory compliance
right from the virtual development process.
The project results show that production
processes can be adapted more quickly,
risks identified earlier, and validation efforts
significantly reduced,” says Rolf van Lengen,
VIMOPROP project manager and Research
Manager for Digital Healthcare at Fraunhofer
IESE.
Virtual Certification as an
Enabler for Pharma 4.0
A key feature of VIMOPROP is the endto-end
integration of quality assurance.
Concepts such as Quality by Design, realtime
quality assurance, and the continuous
monitoring of critical process and quality
parameters during runtime are firmly embedded
in the platform. Simulation results
are automatically checked against defined
quality and performance metrics. On this
basis, virtual certification reports can be generated
that specifically support and accelerate
industrial validation and recertification
processes.
“We developed VIMOPROP so that digital
twins, simulation, and quality documentation
work together seamlessly. Using the
FERAL co-simulation framework, different
models are executed synchronously
and automatically compared against stored
quality and compliance requirements. This
results in transparent and traceable verification
– from the individual module to the
entire production process,” explains Dr.
Jessica Mariño Salguero, an engineer in the
Virtual Engineering division at Fraunhofer
IESE.
The applicability of the approach was demonstrated
using a laboratory-based use
case for media preparation. The results show
how industrial production processes can be
validated virtually and efficiently adapted to
new requirements.
With VIMOPROP, Fraunhofer IESE, together
with its project partners, is creating a
digital foundation for agile, scalable, and regulatory-compliant
pharmaceutical production
and supporting companies in the stepby-step
implementation of Pharma 4.0 into
industrial practice. The project was supported
by the Rhineland-Palatinate Ministry of
Science and Health (MWG) with a grant of
400,000 euros over one year.
Fraunhofer IESE
D 67663 Kaiserslautern
© Fraunhofer IZI / Alernon77 / CoreDESIGN / Ekaterina_1525 - stock.adobe.com
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Leadership change in
materials technology at FBH
Lasers for space applications, power transistors for energy-efficient electronics, or components
for quantum systems – all these developments originate in materials technology.
This is where ultrathin semiconductor layer stacks with precisely defined properties are
created. Using metal-organic vapor phase epitaxy (MOVPE), they are grown in a finely
controlled manner and characterized through comprehensive material analysis. They
form the basis for a wide range of electronic and optoelectronic devices which are developed
both at Ferdinand-Braun-Institut and by external partners and customers for
high-frequency electronics and for photonic applications across the spectrum from UV
to infrared.
Under the long-standing leadership of Prof. Dr. Markus Weyers, the department has
established itself as a high-performance center of expertise for MOVPE. His work has
made a significant contribution to numerous scientific and technological developments
at FBH and to the institute’s growth. He will initially continue to lead his projects, particularly
those on vertically emitting laser chips (VCSELs), and will support his successor
with advice and guidance.
Seamless transition and new impulses
With Dr. Steffen Breuer, an equally distinguished epitaxy expert now takes over leadership.
Following professional positions, for example, at ANU Canberra in Australia, Fraunhofer
IAF in Freiburg, and Fraunhofer HHI in Berlin, he focuses on continuity and innovation
at FBH. “I look forward to continuing the department’s very successful work together
with the outstanding team and to providing new impulses. Highly precise semiconductor
materials form the foundation for many innovative high-tech systems – we aim
to further expand our strengths and align them with future applications,” says Breuer.
The transition is taking place as planned and in close coordination, ensuring seamless
continuity in research, development, and collaboration with partners. The department
will consistently continue its work on innovative material systems for semiconductor
research.
Ferdinand-Braun-Institut gGmbH
D 12489 Berlin
Prof. Dr. Markus Weyers (r.) hands over leadership to Dr. Steffen Breuer. © FBH/P. Immerz
NEWSLETTER | Ausgabe EN 07-2026
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Expands global ASIC services expertise and aims to take on the industry’s
most advanced AI, HPC, mobile and automotive projects
IC-Link by imec joins TSMC 3DFabric®
Alliance to accelerate advanced
packaging and 3D IC innovation
Imec, a world-leading research and innovation hub in advanced semiconductor
technologies, announced that IC-Link by imec, imec’s design and manufacturing
service provider for ASIC and silicon photonics, has joined TSMC Open Innovation
Platform® (OIP) 3DFabric® Alliance. As part of the TSMC OIP ecosystem,
the 3DFabric Alliance enables 3D integrated circuit (IC) innovation, readiness
and customer adoption of TSMC’s 3DFabric, a comprehensive family of 3D silicon
stacking and advanced packaging technologies including TSMC-SoIC®,
CoWoS®, InFO, and TSMC-SoW. Through this partnership, IC-Link will enhance
its capabilities in advanced chip integration, while customers and the expanded
3DFabric ecosystem will be able to leverage imec’s global ASIC services.
The continued growth of AI, high-performance
computing, and memory-intensive
applications push traditional chip design
approaches to their limits. Increasingly, system
performance, power efficiency,
and cost are determined not only by
transistor scaling, but by how multiple
chip components are integrated
into a cohesive system. Integration of
multiple chip components and memory
through advanced packaging
has therefore moved from a backend
consideration to a central element of
chip innovation.
For ASICs this shift demands a new level of
collaboration. Designing leading-edge silicon
and packaging requires co-optimization
through iterative development cycles
between the design, integration, and manufacturing
teams. Through TSMC’s 3DFabric
Alliance, partners gain early access to
2.5D/3D technologies enabling accelerated
solution development. This ultimately will
give IC-Link‘s customers a headstart to develop
3D IC innovation solutions and stay at
the cutting edge of ASICs.
bric Alliance, sending
a clear signal that it is
ready to take on the industry’s most advanced
projects, particularly in Europe and
North America,” said Ozgur Gursoy, Director
Portfolio & Strategy for IC-Link’s ASIC
services. „The collaboration is especially
relevant for companies designing semiconductors
for HPC, automotive, mobile, and
telecommunications markets, where advanced
packaging has become a decisive factor
in performance, power efficiency, and timeto-market.
Through the 3DFabric Alliance,
our customers gain access to advanced
packaging know-how and a smoother path
to high-volume manufacturing and indus-
“Building on imec’s deep expertise in advanced
packaging and heterogeneous integration,
IC-Link now joins the TSMC 3DFatrialization
and still benefit from our flexible
business models.”
„The relentless pursuit of higher performance
and greater power efficiency continues
to drive innovation in advanced packaging
and 3D integration. At TSMC, we actively
collaborate with our 3DFabric Alliance
members to accelerate design enablement
through our transformative 3D IC technologies,”
said Aveek Sarkar, Director of the
Ecosystem and Alliance Management Division
at TSMC. „We welcome imec‘s expanded
collaboration with the
OIP ecosystem through the
3DFabric Alliance and look
forward to working together
to bring even greater value to
the industry.“
IC-Link by imec has been a
TSMC Value Chain Alliance
(VCA) member since 2009
and Design Center Alliance
(DCA) member since 2007
and is now a 3DFabric Alliance
member headquartered
in Europe, underlining
its position as a global key
player in advanced ASIC and
system integration.
This expanded alliance reinforces imec’s
strategic focus on system scaling and heterogeneous
integration, connecting early-stage
research directly with industrial
implementation. As the industry moves
toward modular, multi-die systems, partnerships
like the TSMC OIP ecosystem
and the 3DFabric Alliance will play a key
role in enabling scalable, high-performance
solutions for the next generation of
computing.
IMEC Belgium
BL 3001 Leuven
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The industry is facing an unprecedented wave of regulation: efficiency alone is no longer
sufficient. Companies must ensure safety for employees, seamless product integrity,
and the sustainability of all equipment and processes.
Occupational Safety Guidelines 2026:
Why Stainless Steel is the Backbone
of Modern Industry
From the effective date of the latest updates
to ISO 45001 to the tightening of industrial
safety protocols (such as RD 302/2026),
companies in sectors like the food and
pharmaceutical industries face a fundamental
paradigm shift, for which the choice
of floor conveyors is a decisive factor.
1. Ergonomics: From Recommendation
to Obligation
Work safety inspections in 2026 have increasingly
focused on musculoskeletal disorders
(MSDs). The new regulations have
been intensified and have evolved from
mere recommendations to binding, verifiable
requirements. It is now essential to
avoid tasks that require twisting the torso or
repeated exertion.
— The Inoxtruck solution: Devices such
as the tilting lifter EBT750, the tipping device
EBT10, or the scissor lift truck EXT10
allow the load to be adapted to the operator.
Thanks to this technology, access to the product
is completely ergonomic, eliminating
injury risks and meeting the most demanding
standards for workplace well-being.
2. Microbiological Hygiene
and the New Detergent Regulation
With the introduction of Regulation (EU)
2026/405, cleaning protocols are now significantly
stricter. To meet the European
Green Deal, detergent manufacturers are
replacing conventional surfactants with
new organic formulations. Although more
environmentally friendly, these often require
longer contact times or higher concentrations,
increasing the oxidation risk for conventional
materials such as painted steel.
— The stainless steel advantage: The hygienic
design of Inoxtruck, made with continuous
welds and disinfectable surfaces,
guarantees the absence of dead zones. Our
stainless steel withstands daily deep cleaning
without degrading. This prevents biofilm
proliferation and ensures food safety.
3. Digital Product Passport
and Traceability
Sustainability is at the heart of European
industry in 2026. The new regulatory framework
requires industrial goods to have an
extended lifespan and to be easily traceable
within the circular economy.
— Long-term investment: High-quality
stainless steel ensures fatigue and corrosion
resistance, doubling the lifespan of conventional
devices. This aligns with the goal of
reducing the CO2 footprint of modern production
facilities.
Inoxtruck: Designs of the Present,
Ready for the Future
Compliance with the 2026 regulations
should not be an administrative burden but
an opportunity for process optimization. At
Inoxtruck, we develop material handling solutions
that are not only compliant but also
enhance productivity through absolute hygiene
and advanced ergonomics.
ULMA Lifting Solutions
ES 20560 Oñati · Gipuzkoa
Occupational Safety Guidelines 2026: Why stainless steel is the backbone of modern industry. (Copyright: ULMA Lifting Solutions)
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The feasibility of processing a charge coupled device (CCD) in a 3D NAND-like architecture
paves the way for a cost-effective, high-bit-density memory solution to address the memory wall
for AI specific workloads.
Imec demonstrates the first 3D
implementation of a charge coupled
device for AI memory applications
– Imec presents the first 3D implementation of a charge
coupled device (CCD) with indium-gallium-zinc-oxide
(IGZO) channel, with potential for AI memory
applications.
– Due to the cost-effective fabrication, high bit density,
and block-addressable nature, the 3D CCD device shows
promise to be used as a compute express link (CXL®)
type-3 buffer memory, which is gaining ground for use in
commercial AI memory applications.
– Charge transfer operations were successfully
demonstrated across a 3-word-line-based structure
with vertically integrated IGZO channel.
– “The potential of the 3D CCD device to be used as
a buffer memory lies in its ability to be integrated
in a 3D NAND Flash architecture, which we now
demonstrate for the first time.” – Maarten Rosmeulen,
Program Director Storage Memory at imec.
This week, at the 2026 IEEE International Memory Workshop
(IMW), imec, a world-leading research and innovation hub in advanced
semiconductor technologies, presents a 3D implementation
of a CCD memory device with IGZO channel – a world first. The
functional 3D CCD device consists of vertical memory holes drilled
through a stack of 3 word-lines, serving as phase gates. Transfer of
charges (that make up the bits) across the gates could be demonstrated
at >4MHz transfer speed. The feasibility of processing the
CCD device in a 3D NAND Flash architecture ensures cost-effective
fabrication and bit densities surpassing the DRAM limit. This
makes the block-addressable 3D CCD device an attractive compute
express link (CXL®) type-3 buffer memory for AI use cases – designed
to feed multiple processors with large blocks of data through a
high-bandwidth CXL® switch.
AI’s insatiable hunger for memory is putting significant pressure on
DRAM-based memory technology, which increasingly struggles to
maintain the cost-per-bit scaling trendline. The memory industry
therefore explores alternative, more cost-effective memory solutions
that can complement DRAM and DRAM-based high bandwidth
memory (HBM) for AI-specific workloads. In parallel, new memory
interfaces have emerged that allow for more efficient use of the main
memory resources compared to traditional double data rate (DDR)
buses. One of these is CXL®, a memory protocol designed to make
large pools of memory available to multiple processors through a
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Figure 3 – (a) I-f characteristics from 7 devices with varying memory
hole (MH) diameters, measured up to 4MHz; (b) the number of
electrons transferred per cycle obtained from the slope of the
corresponding I-f curves.
Figure 1 – (a) Schematic of the 3-word-line based 3D CCD structure:
bottom gate (BG), center gate (CG), and top gate (TG), with source (S)
at the bottom and drain (D) at the top; (b) cross-sectional TEM image
showing 3 gate layers with a word-line pitch of 80nm.
Figure 2 – (a) Illustration of the pulsing scheme across 3 gates for serial
charge transfer in a 3-word-line based 3D CCD memory; (b) Schematic
of 3D CCD operation showing electron transfer through the formation
and shifting of potential wells under the gates.
high-bandwidth CXL® switch. These so-called CXL® type-3 buffer
memories have different specifications than DRAM, offering an excellent
opportunity for the introduction of new memory technology.
In 2024, imec conceptually introduced the 3D CCD with an IGZO
channel – offering promising prospects to be used as a CXL® type-
3 buffer memory – and demonstrated memory operation on a 2D
proof-of-concept. Maarten Rosmeulen, Program Director Storage
Memory at imec: “The potential of this CCD device to be used as a
buffer memory lies in its ability to be integrated in a 3D NAND Flash
string architecture – the most cost-effective way to achieve a scalable,
high bit density estimated to go far beyond the DRAM limit. We
now show for the first time a functional 3D implementation with a
3-word-line structure, achieving vertical IGZO channels at dimensions
comparable with what can be achieved for 3D NAND (i.e., 80-
120nm diameter memory holes).”
In the 3D device, the CCD registers – or strings – are integrated into
vertically aligned plugs, which are drilled through the 3-word-line
stack using a 3D NAND-inspired punch-and-plug process. The horizontal
word-lines act as the gates and determine a series of bits
in each string. These bits are based on charges, which can be serially
transferred and stored across the gates using a pulsed voltage
scheme.
“We achieve reliable charge transfer along the vertical IGZO channel
at speeds exceeding 4MHz,” adds Maarten Rosmeulen. “The number
of charges transferred per cycle was measured to be a few thousand,
which is sufficient for one bit or even multibit storage in real memory
applications. Unlike byte-addressable DRAM, our 3D CCD device is
designed to provide block-level data access, which is better suited to
modern AI workloads. These results, in combination with unlimited
endurance, long data retention (ensured by the IGZO channel material),
and low-voltage operation (due to the charge-based nature of
the memory operation) bring the 3D CCD technology a step closer to
buffer memory implementations. In ongoing work, we focus on expanding
the number of word-lines and optimizing the readout stage
of our 3D CCD buffer memory. We are now ready to take our 3D CCD
device technology to the next level with industry partners and fully
unlock its potential for AI memory applications.”
IMEC Belgium
BL 3001 Leuven
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System manufacturers use hotset‘s calibration service for quality assurance
Calibration as a key factor
in process efficiency
Calibrated and with test
certificate: Thermocouples and resistance
thermometers from the extensive range of hotset.
(Image: Hotset GmbH)
The German manufacturer of thermosensors and heating
elements hotset is increasingly establishing itself as a strategic
system partner for measurement and testing equipment
users in machinery and plant engineering. A central
role here is played by the calibration service of the Temperature
Solutions division, which is now used by process engineers,
quality managers, and maintenance personnel across
numerous industries. Read here why a certificate from the
hotset calibration laboratory can be the deciding factor in
optimizing thermal processes.
The calibration laboratory of hotset offers many possibilities
for the metrological testing of temperature sensors in various
temperature ranges. (Image: Hotset GmbH)
The demands on the efficiency of thermal processes are continuously
increasing, and the tolerance limits for temperature measurement
are becoming tighter. In many industries, regular and standard-compliant
calibration of the measurement and testing instruments used
for this purpose has therefore become a central component of quality
assurance. Aside from manufacturers in the refractory industry,
oven construction, process engineering, and heat treatment, it is
the plant builders in the aluminum and steel industries as well as in
automotive and aerospace engineering who increasingly rely on the
services of hotset‘s calibration laboratory. „We are continuously expanding
our technology and competence spectrum so that our Temperature
Solutions division has developed into a recognized service
partner for quality assurance for many machine manufacturers and
plant operators in the field of thermosensor calibration,“ says hotset
CEO Sven Braatz.
Calibration as a Competitive Factor
In companies, it is primarily test technicians, development engineers,
quality managers, and maintenance personnel who are responsible
for monitoring the measurement accuracy of temperature
sensors used in their processes and procedures. To ensure this,
all thermocouples and resistance thermometers used for contact
temperature measurement of solid, liquid, and gaseous media must
be regularly calibrated in accordance with standards. At hotset‘s
calibration laboratory, the measurement deviation of the sensors is
demonstrated and documented by referencing to national or international
standards in accordance with the International System of
Units SI. The testing processes and certificates of the calibration laboratory
adhere to the standards of DIN EN ISO 17025:2005.
For plant builders and assembly manufacturers, calibrating temperature
sensors can be of competitive importance. Typical scenarios
include, for example, when the customer demands proof that only
certified temperature sensors are installed in the machines or devices
they purchase, or when, in the case of maintenance and reengineering
projects, it must be verified whether the existing measurement
systems still meet current tolerance specifications. „With
prolonged operation under high loads, many measuring instruments
lose accuracy, leading to decreased process and product quality as
well as unwanted customer complaints. Regular calibration of sensors
can prevent such negative developments. It ensures that measurement
results are consistently repeatable and accurate,“ explains
Sven Braatz. Especially test technicians, quality managers, and development
engineers in automotive manufacturing, industrial furnace
construction, aerospace, hardening plants, and temperature
technology are increasingly valuing standard-compliant calibration.
„As proof of calibration, we produce acceptance test certificates according
to 3.1 in accordance with DIN EN 10204 or also according to
CQI-9 and AMS 2750G,“ says Helge Meiritz, who heads the Temperature
Solutions division at hotset.
The Temperature Solutions division of hotset represents the company‘s
expertise as a manufacturer of both heating elements and thermosensors.
Under its management, the development, production,
and customer-specific configuration of thermocouples, resistance
thermometers, heating elements, temperature channels, and protective
fittings are carried out. It is often involved in implementing
complex solutions that hotset realizes as a holistic system provider
for customers in industrial temperature control, heating, testing, and
control technology. „Additionally, we also produce thermocouples,
which are integrated solutions combining sensor and measurement
technology,“ emphasizes Helge Meiritz.
Wide Range of Possibilities
Besides calibration as a customer-specific service, hotset also calibrates
the measurement accuracy of thermocouples and resistance
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thermometers from its own product line hotcontrol in its calibration
laboratory. Not only are finished sensors checked, but also all supplier
parts used for their manufacture—such as the sheath material.
The hotset calibration laboratory offers many options for measuring
the temperature sensors at 0°C as well as in the temperature range
from 150°C to 1,200°C, using calibrators, multimeters, multiplexers,
and comparison standards.
device and plant manufacturers worldwide. They are available as
ready-to-use modules in numerous designs and can be used—depending
on the variant—for contact temperature measurement of
solid, liquid, and gaseous media. They are characterized by high
measurement accuracy and fast response times, proving to be longterm
stable, process-safe sensor solutions for temperature ranges
well above 1,000°C in many applications.
Hotset‘s thermosensors are part of the standard equipment of many
Hotset GmbH
D 58511 Lüdenscheid
Vink Chemicals receives EU approval for grotanol® 3025 as a PT 2 disinfectant
Regulatory success
strengthens market
position
Vink Chemicals has achieved another regulatory milestone
and has received EU-wide approval for grotanol® 3025 as
a biocidal product under the Biocidal Products Regulation
(BPR) as a disinfectant of product type PT 2 for CIP and industrial
surfaces.
The approval now granted covers the use of grotanol® 3025 for wiping
and mopping, spray applications (e.g., in tanks), dipping, and
the CIP (Cleaning-in-Place) process – each under clean and dirty
conditions. According to the BPR Regulation (EU) 528/2012, product
type PT 2 includes disinfectants that are not intended for direct application
to humans and animals.
Versatile application in recirculation systems
and production facilities
With EU approval as a PT 2 disinfectant, users benefit from the versatile
possibilities that grotanol® 3025 offers. The product is a mixture
of CMIT/MIT (3:1) (CAS No. 55965-84-9) and glutaraldehyde
(CAS No. 110-30-8), characterized by broad efficacy against bacteria,
yeasts, and molds. The agent produces very low foam, acts quickly,
and can be easily and residue-free rinsed off.
Surfaces that can be disinfected with grotanol® 3025 include, for
example, work surfaces, machinery, equipment, utensils, floors, and
walls, as well as interior surfaces of pipes, containers, filling devices,
mixers, and other machines. This makes the product from Vink Chemicals
relevant for the food and feed industry as well as the metalworking
fluid industry.
Holistic approach supports customers
in implementing hygiene measures
An additional advantage of Vink Chemicals‘ product is its ease of
handling. Furthermore, the ready-to-use solutions of grotanol® 3025
are easily biodegradable and can be disposed of conveniently. The
disinfectant is part of a holistic hygiene concept that emphasizes careful
raw material selection, cleaning, and regular monitoring of the
microbiological status. Vink Chemicals offers biocidal and biocidefree
cleaners and supports its customers with conducting hygiene
audits aimed at preventing potential microbiological contamination.
These steps are also part of the holistic hygiene concept.
The EU-wide approval emphasizes the necessity of having a safe
disinfectant product on the market.
Vink Chemicals
D 21250 Tostedt
Vink Chemicals has received EU-wide approval for grotanol® 3025 as
a disinfectant of product type PT 2 for CIP and industrial surfaces. The
product can also be used for disinfecting interior surfaces of pipes, tanks,
filling equipment, mixers, and other machinery. (Image: Vink Chemicals/
Prostock-studio - AdobeStock_1687943824)
Surfaces that can be disinfected with grotanol® 3025 include
work surfaces, machines, equipment, floors, and walls; the product from
Vink Chemicals is therefore relevant for the food and feed industry
as well as the metalworking fluid industry.
(Image: Vink Chemicals/ Bakha - AdobeStock_1877211690)
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ErP: What is changing now for OEMs, plant builders, and operators
Stricter efficiency
requirements,
clear system boundaries,
and new manufacturer
obligations
With the ErP 2026, the European
Union is significantly tightening the
requirements for fans starting in July.
New efficiency thresholds, revised
assessment methods, and expanded
documentation obligations affect
not only fan manufacturers but also
OEMs, system integrators, and operators.
ebm‐papst informs about the key
changes and shows what users should
prepare for now.
The minimum efficiencies for axial fans have
been gradually increased since 2013. Starting in
2026, a minimum Fan Efficiency Grade of
50 percent will apply – the static total efficiency
at the Best Point is decisive. (Pe = electrical
input power; ηmin = minimum fan efficiency;
ηse = static total efficiency; BEP = Best Point)
(Image: ebm-papst)
The requirements for radial fans with backward-curved
blades are also increasing.
From 2026, the minimum required Fan
Efficiency Grade will be 64 percent, setting a
new efficiency standard. (Pe = electrical input
power; ηmin = minimum fan efficiency;
ηse = static overall efficiency; BEP = best point)
(Image: ebm-papst)
Higher efficiency requirements
– especially under partial load
The new fan regulation significantly raises
the minimum efficiencies and continues to
evaluate efficiency via the Fan Efficiency
Grade (FEG), but based on updated measurement
conditions. New is the stronger focus
on partial load behavior. This shifts the
emphasis from just the optimal point to the
entire efficiency level across the actual operating
range.
The complete fan comes
into focus
For the first time, the regulation clearly defines
when a fan is considered complete.
The decisive factor is the interaction of the
impeller, motor, and stator. Those who complete
incomplete fans or integrate them into
their own systems and market them under
their own name are considered manufacturers
from a regulatory perspective – with all
obligations for conformity assessment and
CE marking.
New obligations for information,
documentation, and repair
The central functional areas of the fan in axial (left) and radial fans (right): the impeller
as the aerodynamic core (green), the motor with integrated electronics as the drive unit (orange),
and the stator, meaning the air-guiding and supporting structures (blue). (Image: ebm-papst)
With ErP 2026, transparency requirements
are also significantly increased. Manufacturers
will need to provide extensive information
on efficiency performance, reparability,
and disassembly. Additionally, defined spare
parts must be available up to ten years after
product discontinuation, while product information
must be maintained digitally for
up to 20 years.
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Timely consideration of
transition periods
The regulation applies from July 24, 2026,
to so-called standalone fans and new products.
For fans integrated into other products
or applications – such as ventilation
units, heat pumps, or refrigeration systems –
and marketed before this date, the requirements
apply from July 24, 2027. Replacement
fans will be subject to clear restrictions from
2027 and may only be used under defined
conditions.
Support from a single source
ebm-papst has been specifically preparing
its portfolio for the requirements of ErP
2026 for years. Fully developed fans, system-related
efficiency assessments, and
transparent documentation make it easier
for customers to switch safely. Additionally,
ebm-papst supports early implementation
of compliant solutions through consulting,
measurements, and digital design
tools.
ebm-papst
Mulfingen GmbH & Co. KGaA & Co. KG
D 74673 Mulfingen
Guideline VDI 2083 Part 4.3
Moisture control in dry cleaning rooms
In some industries, especially in the manufacturing of lithium
batteries, production processes require extremely dry
cleanroom environments. Contamination control by water
presents a central planning and operational challenge.
The VDI expert recommendation VDI-EE 2083 Sheet 4.3 provides
practical guidance for creating and operating areas with dew points
of a maximum of 0 °C, often even -50 °C.
Water as a Contaminant in Pure Environments
Dry cleanrooms are used where even low humidity levels can affect
production processes or materials. Unlike classical particle prevention,
the focus here is on the targeted reduction of water in the air.
The VDI-EE 2083 Sheet 4.3 defines requirements for such areas and
describes the necessary climatic conditions – without addressing
the actual manufacturing processes. It is intended for all professionals
planning and operating such extremely dry clean environments.
Sealing of the Building Envelope as a Key Factor
A central topic of the expert recommendation is the airtightness of
enclosure surfaces and duct systems. Even minor leaks can allow
moisture from the environment to penetrate the controlled area. Removing
this infiltrating moisture requires significant energy expenditure.
Dew points in this area are achieved through adsorption drying.
To prevent damage to the dryers, the release of certain substances,
e.g., from seals, must be avoided. The extreme environmental
conditions also lead to significantly increased wear in tribo-systems.
Corresponding guidance on these points is provided in the VDI expert
recommendation.
The VDI-EE 2083 Sheet 4.3 ‘Cleanroom Technology - Dry Cleanrooms’
was published in January 2026 and can be ordered from DIN
Media for €89.00. Since May 1, 2026, the VDI expert recommendation
has also been available in English.
VDI Verein Deutscher Ingenieure
Postfach 10 11 39
D 40468 Düsseldorf
Telefon: +49 211 6214251
Telefax: +49 211 6214177
eMail: wollstein@vdi.de
Internet: http://www.vdi.de/tga
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New Sustainability Report 2024/2025: Manufacturer of manual
cleaning technology continues to expand sustainable value creation
with more regional supply chains and resource-efficient products
PFENNIG is increasingly focusing
on products from Germany
With more products manufactured in Germany, regionalized
supply chains, and a higher recycled content in the
range, PFENNIG continues its long-standing sustainability
course. The new report documents the current developments
of the Allgäu-based family business.
A key result of the new sustainability report: 16.59 percent of the
products still produced abroad in 2023 are now manufactured in
Germany. A previously set target of 10 percent has been significantly
exceeded. This shortens transportation routes, while simultaneously
increasing supply security and independence from global supply
chains.
Sustainability systematically embedded
“Those who take responsibility seriously must act. Our sustainability
report shows what we have already implemented and what we are
still working on,” says Managing Director Dietmar Pfennig. For over
50 years, PFENNIG has been developing manual cleaning systems
for cleanrooms, healthcare, and professional building cleaning. The
company, headquartered in Durach near Kempten, is now represented
in more than 30 countries. The focus is on solutions that combine
hygiene, quality, and practicality. Sustainability has been part
of the strategic orientation since 2011 and has been systematically
documented since 2022.
To permanently embed the topic of sustainability within the
company, PFENNIG has established an cross-departmental sustainability
team. Employees from various departments develop goals,
support measures, and integrate the topic into existing processes.
Products that conserve resources
PFENNIG is also increasingly focusing on resource-efficient solutions
in its product portfolio. Some cleaning carts already consist of
up to 84 percent recycled material, and the company offers cleaning
textiles with a high recycled content, some even with 100 percent.
The goal: to increase the recycled content in further products as well.
Sustainability also plays a key role in the development of the range.
During the reporting period, PFENNIG implemented more than 50
product developments and optimizations, including considerations
of material use, durability, efficiency, and resource conservation.
Dietmar and Petra Pfennig
In addition to the products, PFENNIG also looks at their use at the
customer’s site: modular cleaning systems and dosing solutions
help reduce water, chemicals, and material consumption during
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Caverion Germany
acquires Kees Klima
und Kältetechnik
cleaning processes while supporting reliable
hygiene standards. Furthermore, according
to the company, 41 suppliers were
evaluated based on sustainability criteria.
Measures to improve energy efficiency at
the site, as well as internal workshops and
training for employees, are also part of the
efforts.
Sustainability can only succeed together
“Sustainable development can only succeed
together with customers, suppliers, employees,
and other partners,” says Petra Pfennig.
Feedback from practical experience and
close collaboration are crucial to realistically
implementing goals and ensuring long-term
progress. “Our course was recently further
validated by external assessments: PFEN-
NIG was awarded the EcoVadis Gold Medal
and is thus among the highest-rated companies
in the international sustainability
rating.”
The full sustainability report 2024/25 can
be read on the company‘s website at https://
pfennig-reinigungstechnik.com/de/nachhaltigkeit.
Caverion Germany will acquire Kees Klima- und Kältetechnik GmbH in Ronnenberg
on May 31, 2026. The company, with nearly 40 employees, specializes in sophisticated
solutions around air conditioning, refrigeration, process, measurement, and
control technology. Industrial companies constitute the largest customer segment.
The acquisition particularly strengthens Caverion in the strategic growth area of refrigeration
and air conditioning technology.
The company, based in the Hanover metropolitan area, achieved a turnover of approximately
EUR 6.1 million in the 2025 fiscal year. The brand Kees Klima- und Kältetechnik
GmbH will remain in existence in the future. The company will be assigned
as an independent branch of Caverion Region North-West. The previous owners, Ulf
Nickel and Jörg Ruhländer, will continue to lead the operational business as managing
directors of Kees Klima- und Kältetechnik GmbH.
„Our growth focus is, among other things, in the field of refrigeration and air conditioning
technology. The company Kees represents a strategic addition to our service
portfolio in this area. Especially in the industrial sector, the company has a very interesting
customer base,“ says Manfred Simmet, CEO of Caverion Germany.
„In recent years, Kees has grown sustainably and profitably. With Caverion as the
new owner, we have the best conditions to continue doing so,“ says Ulf Nickel.
Caverion has set itself the strategic goal of growing also through acquisitions. Following
the purchase of Schulz Lufttechnik and S&A Schaltanlagenbau, the acquisition
of Kees Klima- und Kältetechnik is another important milestone in the ongoing
growth course.
Pfennig Reinigungstechnik GmbH
Heubachstr. 1
D 87471 Durach
Telefon: +49 831 561220
Telefax: +49 831 61084
eMail: info@pfennig-reinigungstechnik.com
www.pfennig-reinigungstechnik.com
Caverion Deutschland GmbH
Riesstraße 8
D 80992 München
Telefon: +49 89 374288117
Telefax: +49 89 374288-520
eMail: Holger.Winkelstraeter@caverion.com
Internet: https://www.caverion.de
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Pharmaceutical service provider awarded the prestigious management prize
for the seventh consecutive time
Vetter achieves platinum status
as a Best Managed Company
– Family business impresses again in all four competition areas
– Site development and digitalization as strategic investment priorities
– New skilled workforce potentials and lifelong learning in focus
Vetter, a partner of global pharmaceutical and biotech companies for
the manufacturing of life-enhancing medicines, has been awarded
the Best Managed Company title for the seventh time. The family
business has thus, as the only company in this year‘s competition,
achieved the platinum status anew. The renowned award is presented
by Deloitte Private, UBS, Frankfurter Allgemeine Zeitung,
and the Federation of German Industries (BDI) to companies for
outstanding performance in leadership and management. The jury
evaluates companies based on four value drivers: strategy, productivity,
culture and commitment, as well as governance and finances.
In 2026, the pharmaceutical service provider receives the award
primarily for the consistent further development of its corporate
strategy and processes in a globally challenging environment. During
a ceremonial award presentation on May 21 at the Palmengarten
Society House in Frankfurt, the trophy and certificate were handed
over to Vetter.
Strategic foresight, active risk management,
and sustainable growth
The jury was particularly impressed by the company‘s consistent and
continuous strategic work: With the successful completion of the
current strategy program Vetter NExT 2029, a solid foundation has
been laid to develop and finalize a new, forward-looking program
this year. The family business also stands out through its clear focus
on achieving ambitious climate protection goals. At the same time,
the further development of integrated corporate reporting and ongoing
risk management enhances the company‘s ability to act. This
enables proactive and reliable action even in times of geopolitical
uncertainties and their potential impacts on supply chains, energy
supply, and other framework conditions.
„The repeated recognition as a Best Managed Company with this
year‘s achievement of platinum status confirms the strength and
resilience of our strategic corporate orientation,“ says Senator h.c.
Udo J. Vetter, Chairman of the Supervisory Board and member of
the founding family. „Our sustainable growth is the result of longterm
thinking and consistent investments in our product portfolio
and the necessary infrastructure. We pursue our goal daily to supply
patients worldwide with important medicines and thus contribute
to improved quality of life.“ Vetter CEO Titus Ottinger adds: „Another
investment focus for us is the digitalization of our value creation
processes. The leverage is significant. Our core claim remains the
same: fewer manual interfaces, more seamless data flows, more data
integrity – without compromises on compliance. This solidifies our
position as a leader in quality and technology and also the long-term
trust of our customers in us.“
Honorary Senator Udo J. Vetter, Chairman of the Supervisory Board and
member of the family of owners (right), and Vetter Managing Director
Titus Ottinger (left) at the award ceremony in the Palmengarten Social
House in Frankfurt. © Vetter Pharma International GmbH
Environmental responsibility and continuous
investments in employees
The jury also praised the clearly defined, ambitious climate goals,
with which Vetter systematically advances the reduction of its CO2
emissions. The pharmaceutical service provider succeeds in combining
ecological responsibility with economic success. Furthermore,
the comprehensive commitment to securing skilled workers and
employee development was highlighted: With innovative approaches
such as the Integrative Entry Program, Vetter unlocks additional
workforce potentials and ensures successful qualification, language
support, and integration. With the company-wide introduction
of the digital learning platform Vetter Learning, the company
consciously emphasizes lifelong learning, knowledge transfer, and
the continuous development of its employees.
Markus Seiz, head of the Best Managed Companies (BMC) program
in Germany at Deloitte Private, emphasizes: „We have been accompanying
Vetter for many years and are continually impressed by how
intensively and consistently management and employees engage in
strategic processes. Moreover, the pharmaceutical service provider
is an outstanding example of how the application process itself can
serve as a complementary catalyst for the company.“
Vetter Pharma International GmbH
D 88212 Ravensburg
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Jury praises strategy, innovation strength, corporate culture, and sustainable
corporate management
Ziehl-Abegg for the third
consecutive
time „Best Managed
Company“
Executives of Ziehl-Abegg are pleased about the award
as „Best Managed Company“. (Photo credit (if necessary): BMCA)
The Ziehl-Abegg SE is once again among Germany‘s best-managed
medium-sized companies. The industrial company was awarded the
„Best Managed Companies Award 2026“ for the third consecutive
time. The award is presented by Deloitte Private in collaboration
with the Federal Association of German Industry (BDI), the Frankfurter
Allgemeine Zeitung, and UBS.
The award ceremony took place at the Frankfurt Palmengarten
Society House. A total of 38 companies nationwide were honored for
demonstrating exemplary corporate management.
In the selection process, an independent jury composed of representatives
from science, business, and media evaluates areas including
strategy, innovation capacity, productivity, corporate culture,
as well as governance and finance.
„The repeated recognition affirms our path. Technology, internationality,
and economic success are important – but what truly
matters are the people within the company,“ says Joachim Ley, CEO
of Ziehl-Abegg SE. „Especially in times of great change, guidance,
reliability, and teams that take responsibility are essential.“
Ziehl-Abegg employs 5,800 people worldwide and is internationally
one of the leading companies in air, control, and drive technology.
Besides technological developments, the company also explores
new avenues in communication, employer branding, and employee
recruitment. Ziehl-Abegg attracts attention through activities
on TikTok, its own e-sports formats, as well as Social Media Days
and the AI Communication Award.
Ziehl-Abegg is making strides with technological innovations
in energy efficiency and sustainability. These include the bionic design
of modern fans and a newly developed ferrite-based elevator
motor that does not require rare earth elements. The innovation was
presented at Hannover Messe 2026 and nominated for the Hermes
Award. The motor achieves the same performance as previous solutions
with neodymium magnets but significantly reduces dependence
on critical raw materials.
The „Best Managed Companies Award“ was founded in the
1990s by Deloitte in Canada and is now awarded in more than 45
countries. Its goal is to highlight and connect successfully managed
medium-sized and family-run businesses internationally.
Ziehl-Abegg SE
D 74653 Künzelsau
Sanner Group appoints Dirk Scholz as the new CFO
Sanner, a globally leading manufacturer of healthcare packaging and CDMO for medical technology products,
has appointed Dirk Scholz as the new Chief Financial Officer (CFO). He joined the company on May 2, 2026.
Dirk Scholz
Dirk Scholz brings extensive expertise and a
track record of more than 30 years in finance
and general corporate management to his
new role. „With his international experience
at private equity-funded companies as
well as large industrial manufacturing firms,
Dirk Scholz is the ideal candidate for Sanner.
He will support us in further advancing
our international growth and positioning
Sanner as a worldwide leading provider of
customized solutions and services in the
fields of medical technology, diagnostics,
pharmaceuticals, and consumer healthcare,“
says Stefan Verheyden, CEO of the Sanner
Group.
Unlocking New Business Potentials
Dirk Scholz adds: „I am very excited to become
part of such an agile and growth-oriented
company whose mission is to provide
customers worldwide with the best possible
CDMO services, reduce complexity, and
enable closer collaboration between development
and manufacturing. The combination
of in-depth know-how in moisture
management and injection molding, as well
as the entire development process of packaging
and devices, is truly unique at Sanner. “
Sanner GmbH
D 64625 Bensheim
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Weidmüller wins the
German Innovation Award with
intelligent interface solution
The ERC from PPC
and Weidmüller wins
in two categories;
„Building & Elements“ and
„Transformative Solutions“.
(Image source: Weidmüller)
The EEBUS Relay Converter receives the Winner Award
from the German Innovation Awards. The product is a joint
development of Power Plus Communications AG and Weidmüller.
It plays a central role in the energy transition and future-proof
grid operation.
Weidmüller receives the German Innovation Award in Berlin for the
EEBUS Relay Converter (ERC). The product wins in the categories
“Building & Elements” and “Transformative Solutions.” The award
recognizes developments that are both socially relevant and economically
effective.
The ERC addresses a key challenge of the energy transition: many
existing systems – heat pumps, PV systems, or charging stations –
still operate analogously, while the overarching power grid is increasingly
controlled digitally. This is where the ERC comes in: it translates
digital EEBUS control signals into analog relay switching commands.
This allows existing systems to be integrated into a smart
power grid without needing to be completely replaced.
This technology is an important building block for the expansion of
smart grids. Grid operators need to be able to control systems flexibly,
for example, to avoid overloads or to optimize the use of renewable
energy. The converter enables targeted control of both power
generators and consumers. Different feed-in power levels can be set
for the power generators.
An additional advantage: the ERC makes it easier to comply with
legal requirements. These include regulations such as § 14a of the
Energy Industry Act (EnWG) and § 9 of the Renewable Energy
Sources Act (EEG), which require controllable integration of systems
into the power grid. Especially because many existing systems
do not yet have a digital control interface, this solution fills an important
gap in the current energy system.
The EEBUS Relay Converter can be operated via a Smart Meter
Gateway with control functions from PPC. It offers secure remote
update capabilities. This ensures the system remains adaptable in
the long term.
L to R: Dr. Joachim Franz Kastner, Program Manager, and
Stefan Oermann, Vice President Global Market Management,
accept the award in Berlin. (Image source: Grand Visions)
“The German Innovation Award confirms our commitment to actively
shaping the energy transition. With the EEBUS Relay Converter,
we create a bridge between existing systems and the digital energy
world, enabling more efficient and future-proof grid operation,” explains
Stefan Oermann, Vice President of Global Market Management
at Weidmüller. With this award, Weidmüller emphasizes its
role as a driver of digital transformation in the energy and industrial
sectors.
Weidmüller GmbH & Co. KG
D 32758 Detmold
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“That was a top interpack. Busy halls, intensive exchange and concrete
projects showed the strength of this global community. interpack
is the most important meeting place for the industry worldwide,
and this edition impressively confirmed that,” said Thomas Dohse,
Director of interpack, at the close of the trade fair.
For seven days, concrete solutions and partnerships took centre
stage. Many discussions led to projects and investment decisions.
The trade fair thus confirmed its role as the leading platform for the
global processing and packaging industry – with strong visitor attendance,
particularly from the food and pharmaceutical industries, as
well as a high quality and density of leading and innovative suppliers.
Market growth – industry under pressure
interpack 2026 took place at a time when the industry is undergoing
transformation. Demand for packaged products continues to
rise, but requirements for materials, production systems and supply
structures are changing. A key focus at the trade fair was the European
Packaging and Packaging Waste Regulation (PPWR), which
marks a turning point for the industry in many respects.
Credit: Messe Düsseldorf / A. Wiese
interpack 2026 sends
a global signal for
the industry
interpack 2026 made the energy of an entire industry truly
tangible. Once again, it became the global meeting place
for the processing and packaging industry and impressively
demonstrated how concrete transformation is already being
implemented in technology, materials and processes.
interpack 2026 sent a clear signal: the packaging industry is more
closely connected, more innovative and more dialogue-oriented
than ever before. This momentum was immediately visible in the
exhibition halls. High visitor traffic, intensive discussions and a consistent
international presence shaped the atmosphere. Everywhere,
it was possible to experience the determination with which companies
are working on solutions for the future. Ideas were discussed,
tested and decisions were made. The entire value chain was presented
in live.
From 7 to 13 May, 2,804 exhibitors from 65 countries and trade visitors
from 161 countries came together in Düsseldorf on the fully booked
exhibition grounds. Of all visitors, 75 percent came from outside
Germany, including 28 percent from outside Europe. Around 100
additional companies were represented at components, the supplier
trade fair held in parallel. This made interpack 2026 the largest edition
in its history in terms of exhibitors, underlining what was clearly
felt in the halls: this was an event with exceptional impact.
interpack made one thing clear: companies are not responding in
isolation, but systemically. Exhibitors presented solutions in which
materials, machines and processes are increasingly considered together
and coordinated with one another. In this way, interpack confirms
its role as an economic driver for the industry: this is where
projects are initiated, investments prepared and economic momentum
generated.
Systems, materials, skills
Automation, data-based applications and flexible plant concepts
have arrived in industrial practice and were presented at interpack
as concrete applications of smart manufacturing. In the field of materials,
the focus was on innovative solutions that work under realworld
conditions and meet regulatory requirements. Future skills
became tangible wherever connected and data-driven systems require
new competencies in production. Personal proximity, shared
experiences and open dialogue gave interpack a special intensity.
Specials provide additional impetus
interpack also set important accents beyond the exhibition stands.
The enhanced specials complemented the trade fair activities and
brought in additional perspectives. The interpack Spotlight Forum,
SAVE FOOD Expert Talks, Women in Packaging, the Start-up Zone
and Young Talents Day showed how broadly the industry’s transformation
is being discussed – from technology and sustainability to diversity,
start-up culture and the promotion of young talent, as well as
qualification and future skills.
What remains is more than a successful trade fair. It is a clear signal:
the industry faces major challenges and is meeting them with innovative
strength, cooperation and the will to actively shape the future.
Added to this is a special combination of international density, technical
depth and a palpable spirit of new beginnings that characterised
this interpack.
The next interpack will take place in 2029. The date will be announced
shortly.
Messe Düsseldorf GmbH
D 40001 Düsseldorf
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Wearable Technologies Conference Europe to be held in Düsseldorf for the first time
– Premiere of the 1st German Health Resilience Conference
MEDICA and COMPAMED 2026: From
innovation to implementation – new topics,
formats and networks for the healthcare
of the future
The healthcare industry is under growing pressure to translate innovation
into care more quickly and consistently. This is precisely where
MEDICA and COMPAMED 2026 come in: as platforms that not
only reflect trends but also enable concrete implementation. With
new themes, programme formats and targeted networking opportunities,
both events are driving forward the transformation process
launched in 2025. The aim is to align MEDICA and COMPAMED, as
leading international community platforms, even more closely with
the demands of an increasingly interconnected, dynamic and decision-driven
market.
At the heart of this is a clear restructuring of content. MEDICA
2026 divides its offering into five precisely defined thematic areas
– ranging from clinical diagnostics and therapeutic technologies,
through digital medicine, data and artificial intelligence, to integrated
care, healthcare infrastructure, and education and global health.
In doing so, the event is consistently geared towards real-world clinical
application scenarios and the concrete needs of healthcare
provision.
“The further development of the thematic structure and the programme
is based directly on feedback from our community. We have
analyzed very carefully which content and formats offer the greatest
added value for our target groups,” explains Carmen Berger, who has
been responsible for MEDICA and COMPAMED at Messe Düsseldorf
since October 2025.
This approach is also reflected in the hall layout. In future, exhibitors
will be positioned more closely in line with specific clinical
requirements and application scenarios. At the same time, the quality
and consistency of content at shared stands will be specifically
enhanced to ensure clear guidance for visitors.
New programme initiatives focus specifically
on exchange and decision-making relevance
Conferences, specialist forums and special exhibitions remain central
components of the live programme – but are being consistently
developed and supplemented by new formats that are more strongly
geared towards interaction, best practices and concrete solutions.
A key new highlight is the Wearable Technologies Conference
Europe, which will take place in future as part of MEDICA in Düsseldorf.
Together with the established Wearable Technologies Show, it
reinforces a field that is becoming increasingly important for the future
of connected healthcare – from prevention and chronic disease
management to telemedical care.
“Wearables play a key role in an increasingly data-driven and
patient-centred care system. With the conference, alongside the innovations
at the WT Show, we are creating a platform for best practices,
professional exchange and new partnerships,” emphasizes
Christian Stammel, CEO of Wearable Technologies AG.
The 1st German Health Resilience Conference marks the first
systematic address of another highly relevant topic for the future.
The focus is on the resilience of healthcare systems and concrete
strategies for dealing with crises and stressful situations – from cyber-resilience
to disaster management and stable supply chains.
“Resilience has long since become a central management task.
Our aim is to bring together decision-makers from different sectors
and discuss concrete solutions,” says Carmen Berger.
Established formats are also being specifically developed further.
The special exhibition “Hospital of the Future” will in future
map the entire clinical patient workflow within a fully integrated system.
At the same time, the MEDICA MEDICINE + SPORTS CON-
FERENCE is moving closer to the heart of the exhibition and will be
integrated with the MEDICA SPORTS HUB to create a closer link
between scientific exchange and the practical application of innovations.
COMPAMED strengthens the technological basis for innovation
MEDICA and COMPAMED are accelerating their transformation process
with new themes, program formats, and networking opportunities
(© Constanze Tillmann/Messe Düsseldorf).
Running parallel to MEDICA, COMPAMED focuses on the technological
foundations of medical technology. As the leading platform
for the supply industry, it brings together expertise in the
fields of manufacturing technologies, components, materials and
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surface solutions.
Furthermore, topics such as regulation, market access, quality
assurance, as well as software, digitalization and cyber security are
gaining further importance – both in the exhibition area and in the
professional programme.
Together, MEDICA and COMPAMED are unique worldwide:
they collectively map the entire MedTech ecosystem – from the initial
idea through development and production to application in healthcare.
This close integration will be further strengthened in 2026,
including through the integration of COMPAMED expertise into selected
MEDICA formats such as the MEDICA TECH FORUM.
Networking is becoming more targeted, relevant
and decision-oriented
There is a particular focus on formats that specifically promote
exchange at the decision-making level. Plans include “Women
in Health by MEDICA”, curated roundtables for political and local
decision-makers, an Investors Lounge for start-ups adjacent to the
MEDICA START-UP PARK (with more than 100 expected participants),
as well as exclusive masterclass meetings and guided tours
with limited participant numbers.
The aim is not only to facilitate contacts, but also to initiate concrete
collaborations and strategic initiatives.
The infrastructure is also evolving
In parallel with the transformation of the event’s content, the exhibition
grounds are also being continuously modernized. The comprehensive
refurbishment of Hall 9, the modernization of the North
Entrance and new conference rooms are part of a long-term master
plan. This is complemented by the construction of a new headquarters
for Messe Düsseldorf – whilst operations continue. Last year,
MEDICA and COMPAMED attracted around 5,300 exhibiting companies
from 70 nations and 78,000 trade visitors from 165 countries.
MEDICA 2026 and COMPAMED 2026 will take place from 16 to 19
November at the exhibition centre in Düsseldorf.
Messe Düsseldorf GmbH
D 40001 Düsseldorf
ASEAN RHVAC
& Cleanroom Industry
Expo (ARHC 2027)
ARHC 2027 will take place on March 17–19 at IMPACT Exhibition
Centre in Bangkok, Thailand. Supported by the Thailand Convention
and Exhibition Bureau (TCEB) and a distinguished network of over
100 leading international and regional trade associations—including
the Council of Engineers Thailand (COE), Malaysian Air-Conditioning
& Refrigeration Association (MACRA), Contamination Control
Society (CCS), Institute of Environmental Sciences and Technology
(IEST), Thai Air-Conditioning Traders Association (TATA), Indoor
Air Quality Association Thailand (IAQ) and Air Movement and Control
Association (AMCA) — ARHC is positioned as ASEAN‘s largest
and most influential HVACR and cleanroom exhibition.
Featured exhibitors include:
Carrier, Daikin, Gree, Midea, Haier, Hisense, AAF International, Bry-
Air, Sanyo Denki, TROX, Nicotra Gebhardt, 3AC, EverCool, Thai Sekisui
Foam, AGF, Huakang, NAPA, TN Group, World Cool, Aoma,
Changsheng, Futai, KLC, Seemtek, Teren, Snyli, Long Long, Greendii,
AAE, A.D.D, SCCE, Skill Development, Takamura, Kaidi, HIRA,
Lairun, Kaiser, and Kriwan, and many more top-tier companies from
across the region.
Building on the huge success of the 2026 edition, ARHC 2027
will showcase advanced HVACR technologies, air filtration and cleanroom
solutions, energy-efficient innovations. As Southeast Asia
undergoes rapid urbanization and industrial upgrades, ARHC continues
to serve as the region’s premier platform for industry collaboration
and cross-border procurement, bringing together a diverse
lineup of global leaders to meet the market‘s evolving demands.
Register in advance as a VIP attendee:
https://wg.hwvips.com/?x=MgjwI9O0O0O7&y=8cd705c42bb33abf23cd44e888a89ea8&isexen=1
ASEAN RHVAC & Cleanroom Industry Expo 2027
IMPACT EXHIBITION CENTRE
11120 Bangkok
Thailand
eMail: grandeur@grandeurint.com
Internet: http://www.aseanhvacexpo.com/
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ASYS Group Redefines AOI
– Autonomous Inspection as a
Key Enabler for Process-Stable
Power Electronics
With the presentation of AISPECTURE AOI – the “World’s first true unsupervised
inspection”, the ASYS Group sets a new technological benchmark in power
electronics manufacturing at PCIM Europe 2026. The solution represents a
fundamental paradigm shift: moving away from supervised, parameter-driven
inspection systems toward a self-learning, AI-led quality authority that ensures
process reliability from the very first component.
The focus of ASYS’s trade show presence
is on manufacturing solutions that address
precisely those areas where conventional
automation reaches its limits: narrow process
windows, increasing product variance,
and the highest demands on reproducibility.
In addition to AISPECTURE, ASYS will
showcase a new generation of inline print
process monitoring for screen printing, as
well as modular automation concepts for
final assembly, specifically tailored to the
requirements of power electronics production.
Autonomous AOI – Rethinking Inspection
Power electronics manufacturing demands
maximum process stability. High power
densities, thermal cycling, new materials,
and long product lifetimes leave virtually
no room for deviation. Especially in printing
and inspection processes, even minimal
deviations have a direct impact on quality,
reliability, and overall cost efficiency. ASYS
addresses these challenges with integrated
process and line solutions designed consistently
for series production capability, scalability,
and statistical stability.
With AISPECTURE AOI, ASYS takes
a decisive step further: the system is not
“operator-free” in the traditional sense, but
AI-autonomous. The underlying algorithms
are deliberately trained using verified, faultfree
print images, from which they develop
a robust understanding of the manufacturing
process. Decisions are therefore not
based on fixed rules or static thresholds but
on context-aware learning and continuous
self-validation – entirely without a humanin-the-loop
during production.
World’s First True
Unsupervised Inspection
AISPECTURE AOI combines real-time
monitoring of the printing process with
automated, high-precision inspection of
the printed result. The system integrates 3D
laser scanning, high-resolution 2D imaging,
and customer-specific AI models. The key
differentiator compared to conventional
AOI systems: no extensive training using
defect images and no manual parameterization
are required.
The result is consistently high inspection
quality from the first part, stable firstpass
yield rates, and a significant reduction
in rework and false decisions. Especially for
high-mix products and small to medium
batch sizes – typical for many power electronics
applications – autonomous AOI
becomes a strategic enabler for stable and
efficient series production.
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HYCON XH2 inline screen printer
with data-driven process control
Complementing inspection, ASYS will present
the HYCON XH2 inline screen printer,
which enables continuous, data-based monitoring
and control of the printing process.
During printing, an integrated piezo sensor
measures the vibration and deformation behavior
of the screen in real time.
The captured signals are continuously
transmitted to the Central AI Box, where
they are analyzed. Changes in signal behavior
allow conclusions to be drawn about the
current screen condition, enabling automatic
adjustment of the process parameters. In
particular, the snap-off is precisely controlled
and adjusted.
The result is consistently high print quality
over extended production periods, along
with a significantly extended screen lifetime
due to reduced mechanical stress. For demanding
power electronics printing applications,
this translates into greater process
stability and reduced scrap.
INVENTUS Assembly Automation:
modular scaling from small batches
to full lines
With INVENTUS Assembly Automation,
ASYS will also demonstrate modular automation
solutions for final assembly. The
platform is designed to grow with the requirements
of power electronics manufacturing
– in terms of production volume, product
variants and complexity.
The range extends from individual modules
and semi-automated workstations to fully
integrated lines and factory-level concepts.
Short ramp-up phases, reproducible processes
and flexible configuration options
support an economically viable transition
from pilot production and small series to
stable series manufacturing.
Focus on process-stable
series production
With its presence at PCIM Europe 2026, the
ASYS Group underlines its approach of delivering
manageable, reproducible manufacturing
processes for power electronics, rather
than isolated machines. The focus is on
the interaction between intelligent inspection,
data-driven process monitoring and
scalable automation – forming the foundation
for reliable products in series production.
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
Released for all countries / Monitoring of proper hand hygiene in the laboratory
Hand Hygiene Training Box
Derma LiteCheck Box
An incorrect disinfection can lead to cross-contamination,
falsified analysis results, or microbiological risks
in the laboratory environment. Therefore, consistent
hand hygiene is an essential part of quality assurance
and occupational safety, with particular emphasis on the
rubbing technique using disinfectants. So-called hand
hygiene training boxes serve as didactic and practical
training systems to teach and verify correct disinfection
techniques.
The Derma LiteCheck Box from BODE Chemie is a tool
for controlling effective hand disinfection and can be
used with any desired hand disinfectant. To prepare a training solution,
the contents of the included Visirub conc. tube are added to a
full 500 ml bottle of Sterillium or 500 ml of another alcoholic disinfectant.
This training solution is used to rub the hands as in routine
hand disinfection. The UV blacklight generated inside the Derma
LiteCheck Box quickly and easily reveals all areas of contact that
resulted from incomplete disinfection. This fast and visually very
impactful fluorescence test achieves an optimal learning effect. The
Derma LiteCheck Box can be quickly and easily used in laboratories,
production, medical and nursing sectors, as well as in training.
The handy training tool Derma LiteCheck Box is delivered folded
and is lightweight and quick to assemble. The dimensions of the folded
box are W 35 x H 35 x D 10.8 cm. Delivery includes power cable,
a tube of Visirub conc., an informational brochure, and labeling stickers.
Please order the desired hand disinfectant separately.
Carl Roth GmbH + Co. KG
D 76185 Karlsruhe
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Handling and transportation of pre-filled syringes (PFS) in nest-and-tube systems
place high demands on conveyor technology. Precise product guidance, maximum
product preservation, and stable process integration are crucial.
Precise conveying technology for
nest & tube systems in pharmaceutical
manufacturing
In automated pharmaceutical production
processes, nest-and-tube systems must be
handled reliably, precisely, and reproducibly.
The goal is to securely feed the sensitive
products into the processing system, continue
processing stably, and minimize mechanical
stresses. At the same time, compact
machine layouts require conveying
technology that can be flexibly integrated
into existing plant concepts. For a machinery
manufacturer in the pharmaceutical
industry, Montech developed a conveying
solution based on the TB30 conveyor belt.
The Swiss technology company has been
specialized for over 60 years in the industrialization
and standardization of advanced
conveyor belts, transfer systems, and aluminum
profile systems.
Process-safe conveying
for sensitive products
For the implementation of this application,
Montech relied on the semi-standardized
TB30 conveyor belts. The conveying solution
combines brushless drives with low-friction
belts, enabling smooth movement of
nest-and-tube systems even with sensitive
products and high process requirements.
For precise product guidance, Montech integrated
side guides specifically developed
for applications in the medical and pharmaceutical
sectors. These can be flexibly adjusted
to different formats and ensure stable
guidance of the products throughout the
entire conveying process. At the same time,
the components used meet high standards
for cleanability and ease of maintenance.
Flexible solution for
demanding applications
The modular design of the conveyor belts
allows easy integration into existing machine
and plant concepts. This enables
space-saving and efficient realization of
both infeeding and outfeeding processes.
Especially for machinery manufacturers, the
combination of standardized components
and customer-specific customization offers
advantages; project planning times can be
reduced, and individual requirements can
still be implemented flexibly. At the same
time, the short delivery times and high configurability
of Montech‘s solutions ensure
cost-effective realization of demanding applications
in pharmaceutical and medical
technology.
NEST Lösung
Montech AG
Gewerbestrasse 12
CH 4552 Derendingen
Telefon: +41 326815500
eMail: info@montech.com
Internet: https://www.montech.com
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MedGuard®: more than packaging
– an integrated system for safe and
sustainable sterilization barrier solutions
SÜDPACK Medica provides a comprehensive packaging
system with MedGuard®, designed to support manufacturers
in medical technology, pharmaceuticals, and life sciences
in selecting and implementing their packaging concepts.
Under MedGuard, the packaging specialist combines
different material structures with process expertise to create
validated packaging solutions that focus on performance,
product and process safety, and not least, sustainability
throughout the entire lifecycle of the packaging.
requirements and common sterilization methods – such as steam,
EtO, or gamma – thereby reducing development times and minimizing
risks in packaging development. (to the Product Navigator)
Manufactured in cleanroom conditions
The MedGuard portfolio includes flexible and rigid packaging systems
– from robust thermoformed films to pouch and bag solutions.
Special lid materials are produced in certified cleanroom environments
to meet requirements for clean production and validated sterile
packaging (e.g., according to ISO 11607).
Strong partnerships across the entire value chain
For consistent system compatibility, SÜDPACK Medica collaborates
with selected manufacturers of paper and lid materials as well
as leading packaging machine manufacturers. This enables targeted
design, testing, and optimization of seal performance and opening
behavior for the machinery platforms used in industry.
Comprehensive in-house laboratory capabilities also allow precise
measurement of mechanical, thermal, and functional film properties
to support customer-specific requirements and validation
processes.
Technical validation at the Ochsenhausen testing center
With MedGuard, SÜDPACK Medica pursues a systematic approach:
instead of individual materials, customers receive an integrated solution
consisting of bottom and lid films or pouch systems, paired
with production and application knowledge, as well as a structured
assessment of sustainability performance. The goal is reliable performance
throughout the entire lifecycle of the packaging – from
development and qualification to commercial scale-up. „More than
packaging. It’s a system.“ Under this guiding principle, MedGuard
addresses key requirements of the healthcare industry: sterile barrier
systems, reproducible sealing processes, regulatory compliance, and
an increasing demand for circularity of packaging concepts.
Quickly find the right material combination:
Product Navigator
With the Product Navigator, SÜDPACK Medica supports material
selection in an increasingly complex environment. Users can evaluate
suitable material combinations based on specific application
Additionally, SÜDPACK Medica offers its customers the option to
conduct seal tests with MedGuard films combined with various lid
materials at the testing center in Ochsenhausen. These tests enable
targeted evaluation of seal windows, peel performance, and process
robustness – supporting packaging development before commercial
scale-up. When necessary, SÜDPACK Medica also coordinates joint
optimization tests with the customer and their machinery suppliers.
Sustainability based on lifecycle analyses
Sustainability is also embedded in the MedGuard strategy: The
sustainability department at SÜDPACK Medica conducts screening
LCAs among other activities to quickly obtain environmental
assessments based on secondary data and ensure that the
packaging systems deliver the best sustainability performance in
their class – without compromising safety, functionality, or regulatory
compliance.
SÜDPACK Medica AG
CH 6341 Baar
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Measure concentrations inline in processes such as SC1, SC2 and BOE
New ultrasonic sensor
from SensoTech for
semiconductor
wet processes
The new SensoTech
sensor enables continuous inline
monitoring of chemical concentrations in
semiconductor wet processes. (Image: SensoTech GmbH)
New sensor technology measures critical chemicals directly
in the running process and helps semiconductor manufacturers
detect process deviations earlier, reduce (lab) effort
and run wet processes more stably.
In semiconductor manufacturing, reliable, controlled wet processes
determine yield, quality and reproducibility. Especially in process
steps such as SC1, SC2 or BOE (Buffered Oxide Etch), chemical concentrations
must be maintained precisely, because even small deviations
can negatively affect cleaning and etch results. With a new sensor
designed specifically for the semiconductor sector, SensoTech is
now bringing an ultrasonic solution to the market that enables these
concentrations to be monitored directly inline and in real time.
Inline measurement for critical cleaning
and etching processes
The focus is on classic and modified SC1 and SC2 chemistries in wafer
manufacturing, specifically NH₄OH / H₂O₂ / H₂O and HCl / H₂O₂
/ H₂O, not only in standard mixes, but also in process-specific dilutions,
concentration windows and adapted recipes (e.g. with TMAH).
The same applies to BOE (BHF) based on HF and NH₄F, where even
minor deviations can influence etch rate, selectivity and process stability.
The new sensor was designed precisely for these chemically
sensitive wet processes.
Everyday challenge: Monitoring process
chemistry reliably and cost-effectively
The target audience is primarily semiconductor manufacturers,
operators of wet benches and wet-process tools, as well as process,
equipment, integration and quality engineers who must ensure chemical
process stability in the cleanroom. Their day-to-day work is
shaped by tight process windows, high quality pressure, limited cleanroom
space and the need to monitor chemical compositions with
as little additional sampling or manual handling as possible. Inline
analysis solutions already exist for these tasks, but they are often
based on more complex measurement methods and are therefore
demanding to integrate and operate. This is exactly where the new
sensor comes in: Instead of relying on time-delayed lab analyses or
complex analytics, concentration information is available immediately
within the process.
Ultrasound-based, temperature-compensated
and prepared for straightforward integration
The SensoTech solution uses ultrasonic transit time, i.e. the specific
speed of sound in the medium, as the central measured variable for
determining concentration. Depending on the medium and process,
this principle can be combined with additional parameters such as
conductivity or other process-relevant variables. The system consolidates
the available measurement signals, compensates for temperature
effects and calculates the relevant concentration information
from them in real time. This creates a flexible measurement architecture
for different wet processes without complicating integration.
The system is completely maintenance-free, requires no consumables
and can be integrated into existing automation environments
via standard interfaces.
More control over critical wet processes
The controller visualizes the inline-measured concentrations
of, for example TMAH and H₂O₂ as well as the process temperature,
in real time. (Image: SensoTech GmbH)
The new solution is particularly relevant wherever stable chemical
concentrations directly determine process quality and tool
availability. In SC1 and SC2 baths, this concerns the reliable adherence
to specified recipes, in BOE processes, it additionally
involves the precise control of a particularly sensitive etching
medium. Continuous concentration monitoring provides a robust
data basis for detecting process deviations early, assessing
bath lifetime more specifically and aligning maintenance inter-
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ventions and chemical management more closely with the actual
process condition.
Direct benefits for production and process control
For operators of wet-process tools, this primarily means more
confidence in day-to-day process control. Concentration trends
become transparent, process windows can be maintained more
stably and changes in bath condition can be assessed earlier.
This supports reproducible tool operation, reduces unnecessarily
conservative bath changes and improves the foundation for
quality assurance, documentation and ongoing process optimization.
SensoTech GmbH
D 39179 Magdeburg-Barleben
Cable Glands and
Accessories for
Every Area of
Application
Wherever cables or lines are run through an enclosure wall,
strain relief and sealing are required. Ganter now offers the
right cable glands and accessories in three thread types.
Cable glands are proven standardized parts that are now available
from Ganter in many different sizes and with various types of thread.
The standard parts with part number GN 62444 are indispensable in
mechanical engineering and plant construction and are used anywhere
that cables, hoses, or lines must be run through an enclosure
or separating wall. Examples include switch cabinets, welding machines,
battery storage systems, and e-charging stations, just to list
a few. In all cases, these parts secure cables at the plane of entry to
provide effective strain relief and sealing – in the cable glands from
Ganter, this is achieved with a durable and reliable sealing and clamping
insert made of chloroprene rubber.
Ganter offers cable glands with clamping diameters from 3 to 44
mm and three types of thread: metric types in the dimensions M12
to M63, PG 7 to PG 48, and – specially for the US market – inch-based
NPT thread with tapered profile. While PG thread has long since
been replaced by metric standard dimensions, PG thread connections
remain indispensable for solving real problems in the repair,
retrofitting, or modification of older systems. Ganter offers all three
types in gray polyamide as well as in brass and (except for the NPT
versions) in stainless steel for corrosive environments. For most applications,
the plastic version is the first choice and offers the best
cost-benefit ratio. In applications where rough conditions and higher
loads are encountered, Ganter recommends the high-quality
metal versions.
Naturally, the matching accessories can also be ordered from Ganter:
Thin mounting nuts GN 62444.1 of brass, plastic, or stainless steel
secure the fittings when thin-walled enclosures or bulkhead panels
permit only unthreaded through holes.
Threaded plugs GN 62444.2 of brass or plastic securely seal existing
enclosure holes that are not currently needed.
Multiple sealing inserts GN 62444.3 of thermoplastic elastomer
allow for up to eight individual cables to be run together through a
standard cable gland, making them extremely efficient in terms of
space, time, and cost.
Reducers GN 62444.4 enable the use of smaller cable glands, such as
where standard enclosures holes are too large.
Otto Ganter GmbH & Co. KG
Triberger Straße 3
D 78120 Furtwangen
Telefon: +49 7723 65070
Telefax: +49 7723 4659
eMail: info@ganternorm.com
Internet: http://www.ganternorm.com
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Under-counter devices with glass door variant and touch display in two versions
/ Awarded the iF Design Award 2024
Networkable laboratory washers
with chamber lighting and enhanced
user convenience from
Miele Professional
Control functions for safe
program operation
A patented, variable-speed circulation
pump automatically adjusts the water pressure
according to the load. A spray arm and
rinse pressure control additionally monitor
the program process and detect, for example,
blockages caused by large vessels or pipettes.
The EasyLoad accessory system with
suitable loading carriers ensures safe and
quick loading for different types of laboratory
glassware.
Two systems for drying
In medical and analytical laboratories,
glassware must be cleaned quickly, reliably,
and residue-free. To meet this requirement,
Miele Professional has developed
its new generation of laboratory washers.
The 60 and 90 centimeter wide undercounter
units are networkable, feature an
illuminated wash chamber, and can be
operated intuitively via a new touch display.
Two systems are available for subsequent
drying.
Even before market launch, the design of
the devices was awarded the iF Design
Award 2024. Contributing to this was,
among other things, the standard rinse
chamber lighting, which significantly facilitates
loading and unloading. The devices
are optionally available in white or stainless
steel. The top models, with a width of
90 centimeters, are additionally available
with a glass door – so the laboratory glass
remains visible throughout the entire washing
process.
The ExploreLine device PLW 8604 already
offers extensive basic equipment including
a touch display. Programs can be quickly selected,
and the current status is always visible.
The ExpertLine devices go even further:
their 4.2-inch color display with M Touch
Flex control shows program status and process
steps clearly visible even from several
meters away.
At the same time, the user interface supports
laboratory staff with recurring tasks. Graphic
hints indicate, for example, which steps are
required next. This simplifies handling and
helps avoid downtime.
Up to 19 programs are available, including
programs for pasteurization or thermal
disinfection. Additionally, up to ten free
program slots can be set up for individual
requirements. The „Extra Short“ program
works especially quickly: up to 60 laboratory
glasses are cleaned in just 25 minutes.
For particularly resource-efficient
operation, there is also the „Standard Eco“
program, which reduces water and energy
consumption.
Two variants are available for drying. Devices
with active drying dry the wash items
directly inside the unit. Alternatively, there
are models with an AutoOpen function: after
the program ends, the door opens automatically
once the temperature in the wash
chamber has sufficiently decreased. Residual
moisture escapes quickly, and the laboratory
glass dries promptly. In most devices, a
steam condenser expels the remaining moisture
outside.
Networkable and service-friendly design
All new laboratory washers are networkable
from the factory. Using the Miele MOVE
Connect software, they can be connected
to a PC, tablet, or smartphone. Performance
data, programs, and consumption values can
thus be viewed and documented centrally.
Maintenance and service were also considered
during development. Central components
are arranged so that Miele service can
reach them faster than with the previous
generation. Maintenance work can therefore
be carried out significantly more quickly.
The devices are designed for at least 15,000
operating hours. Spare parts remain available
for at least 15 years. This makes the Miele
Professional laboratory washers reliable and
durable partners in daily laboratory work.
Miele & Cie. KG
D 33332 Gütersloh
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www.reinraum.de | www.cleanroom-online.com NEWSLETTER | Ausgabe DE 05-2023 Seite 67/103
Veranstaltungen im Juli 2026
Für mehr Informationen oder zum Anmelden einfach auf die Veranstaltung klicken
16.07.2026 Seminar Hygiene
Veranstaltungsort: Affoltern am Albis, Veranstalter: PTS Training Service
Veranstaltungen im August 2026
Für mehr Informationen oder zum Anmelden einfach auf die Veranstaltung klicken
25.08.2026 Seminar Reinraum Praxisseminar inkl. Workshops
Veranstaltungsort: Rheinfelden (CH), Veranstalter: Swiss Cleanroom Concept GmbH
26.08.2026 Seminar Qualifizierung von Anlagen und Utilities
Veranstaltungsort: Rheinfelden (CH),Veranstalter: Swiss Cleanroom Concept GmbH
27.08.2026 Seminar Kontaminationskontrollstrategie sinnvoll umsetzen
Veranstaltungsort: Rheinfelden (CH), Veranstalter: Swiss Cleanroom Concept GmbH
Veranstaltungen im September 2026
Für mehr Informationen oder zum Anmelden einfach auf die Veranstaltung klicken
01.09.2026 Seminar GMP-gerechte Kalibrierung
Veranstaltungsort: Mörfelden-Walldorf, Veranstalter: Testo Industrial Services GmbH
01.09.2026 Seminar Anforderungen an Single use Systeme
Veranstaltungsort: Rheinfelden (CH), Veranstalter: Swiss Cleanroom Concept GmbH
01.09.2026 - 03.09.2026 Seminar Pharma-Ingenieur/in (PT 25) - Block I
Veranstaltungsort: Heidelberg, Veranstalter: CONCEPT HEIDELBERG GmbH
02.09.2026 Seminar Das Kalibrierzertifikat
Veranstaltungsort: Mörfelden-Walldorf, Veranstalter: Testo Industrial Services GmbH
02.09.2026 Seminar Anforderungen an die Sterilisation
Veranstaltungsort: Rheinfelden (CH), Veranstalter: Swiss Cleanroom Concept GmbH
03.09.2026 Seminar Sicherer Umgang mit Zytostatika
Veranstaltungsort: Allschwil BL (CH), Veranstalter: Swiss Cleanroom Concept GmbH
07.09.2026 Symposium 1. Swiss Cleanroom Symposium
Veranstaltungsort: Pratteln (CH), Veranstalter: Swiss Cleanroom Concept GmbH
08.09.2026 Seminar Learnings durch den neuen Annex 1
Veranstaltungsort: Rheinfelden (CH), Veranstalter: Swiss Cleanroom Concept GmbH
09.09.2026 - 10.09.2026 Training & Schulung GMP-Reinraumschulung für aseptische Bereiche
Veranstaltungsort: Osnabrück, Veranstalter: Piepenbrock Dienstleistungen GmbH + Co. KG
09.09.2026 Seminar Fortbildung zum Reinraum-Manager
Veranstaltungsort: Rheinfelden (CH), Veranstalter: Swiss Cleanroom Concept GmbH
09.09.2026 - 10.09.2026 Konferenz Jahresforum Reinraum
Veranstaltungsort: Wien (AT), Veranstalter: imh GmbH
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Veranstaltungen im September 2026
Für mehr Informationen oder zum Anmelden einfach auf die Veranstaltung klicken
15.09.2026 - 17.09.2026 Seminar Umgang mit Abweichungen in der Sterilproduktion (S 9)
+ Mikrobiologisches Umgebungsmonitoring (S 6)
Veranstaltungsort: Karlsruhe, Veranstalter: CONCEPT HEIDELBERG GmbH
16.09.2026 - 17.09.2026 Konferenz Konferenz Reinraum
Veranstaltungsort: Wien (AT), Veranstalter: imh GmbH
16.09.2026 - 17.09.2026 Seminar Bestimmung von Messunsicherheiten nach GUM
Veranstaltungsort: Online, Veranstalter: Testo Industrial Services GmbH
16.09.2026 - 18.09.2026 Seminar Validierungsbeauftragte/r in der pharmazeutischen Industrie (QV 16)
Veranstaltungsort: Mannheim, Veranstalter: CONCEPT HEIDELBERG GmbH
21.09.2026 - 25.09.2026 Seminar Kalibriertage Thermodynamik:
Prüfmittelmanagement und Kalibriertraining
Veranstaltungsort: Wien (AT), Veranstalter: Testo Industrial Services GmbH
22.09.2026 Seminar GMP-Grundlagen für Neueinsteiger
Veranstaltungsort: Rheinfelden (CH), Veranstalter: Swiss Cleanroom Concept GmbH
23.09.2026 - 24.09.2026 Messe Ilmac Lausanne 2026
Veranstaltungsort: Lausanne (CH), Veranstalter: MCH Group AG
25.09.2026 - 26.09.2026 Seminar Sicherheitstraining Zytostatika
Veranstaltungsort: Elmshorn, Veranstalter: Berner International GmbH
29.09.2026 - 30.09.2026 Workshop Praxisworkshop Reinigungsvalidierung
Veranstaltungsort: Kirchzarten bei Freiburg, Veranstalter: Testo Industrial Services GmbH
29.09.2026 - 01.10.2026 Messe POWTECH 2026
Veranstaltungsort: Nürnberg, Veranstalter: NürnbergMesse GmbH
29.09.2026 Seminar Praxis-Seminar für neue Teammitglieder:
Kontaminationskontrolle und Arbeiten im Reinraum
Veranstaltungsort: München, Veranstalter: comprei Reinraum-Handel und Schulungs GesmbH
30.09.2026 - 11.12.2026 Training & Schulung Lehrgang zum zertifizierten Reinraumexperten | 3 Module 3x3 Tage
Veranstaltungsort: Kempten, Veranstalter: comprei Reinraum-Handel und Schulungs GesmbH
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:
Die namentlich gekennzeichneten Beiträge stehen in der Verantwortung des jeweiligen Autors. Nachdruck, auch auszugsweise, nur mit Genehmigung
der Redaktion und mit Quellenangabe gestattet. Für unaufgefordert eingesandte Manuskripte und Abbildungen übernimmt der Herausgeber keine
Haftung. Dem Herausgeber ist das ausschließliche, räumliche, zeitliche und inhaltlich eingeschränkte Recht eingeräumt, den Beitrag in unveränderter
oder bearbeiteter Form für alle Zwecke beliebig oft zu nutzen oder Dritten zur Nutzung zu übertragen. Dieses Nutzungsrecht bezieht sich auf Print- und
elektrische Medien (Internet, Datenbanken, Datenträger aller Art).
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