Supplier Quality Guidelines - Heinrich Huhn GmbH & Co.

Heinrich Huhn GmbH + Co. KG
Hauptstrasse 44
D-57489 Drolshagen-Huetzemert
Germany
Phone: +49 (0)2763 81-0
Supplier Quality Guidelines
HUHN PressTech spol. s.r.o
Školská 1604/30
95201 Vráble
Slovak Republic
Phone: +421 (37)77 686-0
HHR 001, revision level 12/10 Supplier Quality Guidelines Page 1 of 13

Table of Contents
1 Introduction
1.1 Scope
1.2 Target Agreement
1.3 Document Priority / Hierarchy
2 Quality and Environmental Management System Requirements
3 Auditing
3.1 Audits
3.2 Evaluation
4 Product/Process Development
4.1 HUHN-Specific Products/Processes
4.2 Standard Products
5 Production Process and Product Approvals
5.1 First Article Samples
5.1.1 HUHN-Specific Components
5.1.2 Standard Products
5.2 Approval
6 Re-Qualification
7 Required Duration of Records Retention
8 Machines and Process Capabilities
9 Traceability
10 Environment and Utilised Materials
11 Changes
12 Shipments
13 Defective Parts
13.1 At the Supplier’s Facility
13.2 At HUHN’s Facility
13.3 At the Facility of one of HUHN’s Customers
14 Ongoing Measures During Series Production
15 Mandatory Insurance
16 Secrecy
17 Use of Sub-Suppliers
18 Additional Freight Charges
19 Term of Validity
20 Terms and Conditions of Purchase
21 Revisions
22 Informations
HHR 001, revision level 12/10 Supplier Quality Guidelines Page 2 of 13

1 Introduction
The customers of Heinrich Huhn GmbH + Co. KG and Huhn PressTech spol., s.r.o. (hereinafter referred
to as HUHN) are renowned system suppliers and automobile manufacturers.
HUHN has set itself the goal of exceeding the expectations of its customers with regard to on-time
delivery of top quality, defect-free, environmentally sound products at competitive prices.
Continuously impeccable quality and reliability of purchased parts, materials and services, as well as
substantiated process and quality capabilities on the part of the supplier, make a considerable
contribution to this goal. The quality provided by our suppliers is thus an integral part of HUHN’s product
excellence, thus making it necessary for HUHN to fully incorporate its suppliers into its own management
system.
For this reason, we involve our suppliers in quality planning for new projects at the earliest possible stage.
We endeavour to continue our own development in partnership with the best possible suppliers –
because we will only be able to master the future mutually by supplying above average services.
Technical Director Quality Manager
Director of Procurement Purchasing Manager
Please feel free to contact us at any time with questions or suggestions for improvement.
HHR 001, revision level 12/10 Supplier Quality Guidelines Page 3 of 13

1.1 Scope
This quality assurance agreement is based upon DIN EN ISO 9001, VDA publications and ISO TS 16949,
as well as requirements set forth in DIN EN ISO 14000 ff. and the Eco-Management and Audit Scheme
(EMAS).
As a supplement to our general terms and conditions of purchase, the referenced processes and
sequences are an integral part of all supply contracts entered into by HUHN and its suppliers, and is valid
for both HUHN facilities.
HUHN expects its suppliers to implement all described processes and methods continuously and
consistently, and to fully comply with all specified requirements.
The supplier is fully responsible for the quality of supplied parts, materials and services.
1.2 Target Agreement
HUHN invariably expects “zero defects” from its suppliers, which our customers also demand from us. It
is the duty of the supplier to firmly establish this objective within his quality management system, and to
align all processes to it.
In order to support this process, HUHN will establish realistic action limits together with the supplier if
necessary, and monitor goal achievement by means of a periodic comparison of the actual situation with
target values.
In the event of deviation from target values, corrective measures must be implemented by the supplier
and HUHN must be notified.
1.3 Document Priority / Hierarchy
In the event that various documents contain contradictory entries, HUHN must be notified in writing
without delay. Component specifications, delivery specifications and performance specifications have
priority over all other documents.
2 Quality and Environmental Management System Requirements
Adequate quality capability necessitates the maintenance of an up-to-date, effective quality management
system by each and every HUHN supplier. For this reason, the supplier must set up and verify a quality
management system which complies at least with DIN EN ISO 9001:2000.
Beyond this, HUHN expects its suppliers to be prepared to update their own QM systems as the standard
itself is revised to approximate TS 16949 more closely, and to accommodate and continuously improve all
aspects of an environmental management system in accordance with DIN EN ISO 14001 or the Eco-
Management and Audit Scheme (EMAS).
Certification from an independent authority or an environmental consultant, as well as recent system and
process audit reports issued by automobile manufacturers or system suppliers if deemed appropriate by
HUHN, may be submitted as substantiation of the status of the supplier’s management systems.
Companies related to special processes like hardening, galvanizing, welding or soldering are requested
to document CQQ (AIAG)-requirements in a sufficient way. HUHN reserve the right to ask for transmitting
the relevant documents temporarily.
HHR 001, revision level 12/10 Supplier Quality Guidelines Page 4 of 13

3 Auditing
3.1 Audits
In the case of suppliers who are not yet certified in accordance with DIN EN ISO 9001, VDA 6.1, QS-9000
or ISO TS 16949, or who are unable to substantiate a successfully completed audit conducted by an
automobile manufacturer or a renowned system supplier, HUHN will conduct an examination or potential
analysis if applicable regarding the status of HUHN’s requirements with respect to the supplier’s quality
management system (supplier audit).
The supplier shall grant HUHN access to its facilities, as well as review of its documents and processes
by previous appointment to this end. During the course of the supplier audit, HUHN may incorporate
elements from regulatory frameworks including VDA 6.3, CQI 09-15 (AIAG) , customer specifications or
its own requirements.
In the case of suppliers who are certified in accordance with the above mentioned criteria, HUHN will, as
a rule, not conduct a supplier audit, but will rather limit itself to a process or product audit if necessary.
In the event of a process audit, the process sequence is observed and examined with regard to
planning, development and production of a product which HUHN intends to purchase, to determine
whether or not all requirements for error-free manufacturing of the product have been fulfilled.
Reasons for process audits may include:
� Verification of the product development process and the initial phase of large-scale production
(new products)
� Quality problems after delivery to HUHN
� Process optimisation
� Process changes
� Moving the process to a different location
The results of the audit demonstrate the supplier’s quality capability. In the event that deviations (defects)
are detected, an action plan must be prepared by the supplier and approved by HUHN. The defects must
be eliminated. HUHN reserves the right to convince itself that this process has been successful by
auditing the implementation of corrective measures.
Audit results and knowledge gained during the facilities tour shall be treated confidentially, and shall not
be made available to any third party or parties by HUHN, unless such transmission is expressly approved
by the supplier.
3.2 Evaluation
The results and findings of the audit shall be evaluated by HUHN’s auditors, and assessed in accordance
with VDA guidelines. The supplier is then assigned to one of the following supplier relationship categories:
� Suppliers assigned to category A (≥ 90%) are approved without restriction.
� Suppliers assigned to category AB (≥ 80%) are approved with certain restrictions. The supplier
must eliminate deviations detected during the audit within a specified period of time.
� Suppliers assigned to category B (≥ 60%) are only permitted to ship goods in exceptional cases.
Such exceptional cases are defined by HUHN as required.
The supplier must eliminate deviations detected during the audit within a specified period of time, in
order to achieve a rating of at least AB.
� Suppliers with results of less than < 60% are disbarred.
Supplier approvals (categories A and AB) do not simultaneously constitute production approval.
Production approval is an integral part of the product/component approval described below. It must be
requested by the supplier as part of the first article submission process. The supplier approval indicates
that the supplier is capable of manufacturing products in accordance with HUHN’s quality requirements.
HHR 001, revision level 12/10 Supplier Quality Guidelines Page 5 of 13

4 Product/Process Development
4.1 HUHN-Specific Products/Processes
HUHN strives to involve the supplier in the developmental process as early as possible. This applies in
particular to application-specific products/processes.
By means of mutual development (within the framework of simultaneous engineering) and close cooperation
from the product development stage right on up to initial series production, not only are R&D times reduced,
qualitatively and economically optimised solutions are created as well for both companies. Potential sources
of error can be avoided by implementing appropriate measures during the R&D phase, and prerequisites for
technically stable, reliable manufacturing processes can be fulfilled.
Objectives of cooperative work include:
� Reduced R&D time and costs
� Realisation of the most cost-effective solution
� Top quality, durable and especially environmentally sound products
� Minimisation of the risk of error
� On-time launch of series production with technically mature products
� Avoidance of product liability risks
HUHN provides the supplier with all necessary information.
In particular this includes:
� Specification (drawings, delivery specifications etc.)
� Intended purpose
� Special and particularly important features for functions and assembly
� Packaging and shipping requirements
The supplier must make the following contributions during product/process development:
� Suggestions which serve to:
– Avoid potential errors
– Reduce costs
– Improve the product
– As well as suggestions for special and important characteristics within the framework of the
supplier’s design/process FMEA
HUHN carefully examines these suggestions and corrects the affected specifications accordingly if
necessary, in accordance with customer requirements if applicable.
� Feasibility studies
� Design tests (engineering tests, design certification)
� Design FMEA
� Process planning
� Process FMEA
� Process capability analyses and substantiations
� Process validations (qualifications)
� QM plan (inspection plan): As a rule, a plan must be prepared and submitted for the following 3 phases:
– Prototypes
– Pre-production series
– Series production
� Test equipment planning
� Production equipment planning
� Packaging suggestions
Completed records subsequently become an integral part of first article inspection documentation. Records
must always be kept in German, although another language or a translation may be agreed upon within the
framework of the respective project.
When the project is launched, the product/project timetable must be coordinated with HUHN. The supplier
HHR 001, revision level 12/10 Supplier Quality Guidelines Page 6 of 13

must inform HUHN on a regular basis regarding developmental progress (status report). Reviews are
conducted with the supplier at agreed upon intervals.
The project manager (APQP champion) must be appointed by the supplier, and agreed upon separately in a
product-specific fashion if applicable.
4.2 Standard Products
Standard products are parts, materials and processes, which a supplier develops, produces and documents
independently for the market.
HUHN must be informed regarding the results of product development, as well as the product genesis
process. This must take place within the framework of the first article submission process
The supplier must confirm compliance of his product with HUHN’s delivery specification. Deviations must be
approved by HUHN.
If standard products are selected (e.g. limitation of parameters), they must be confirmed by the supplier and a
part number (article number) must be generated. The process capability of the limited characteristics must be
substantiated to HUHN.
5 Production Process and Product Approvals
5.1 First Article Samples
5.1.1 HUHN-Specific Components
The supplier must submit a first article sample punctually before approval for series production is issued. The
first article sample and first article inspection reports are an integral part of orders placed by HUHN.
Unless otherwise specified, submission of the first article inspection report must be made in accordance with
respectively valid stipulations per QS-9000-PPAP (production part approval process), level 3, or VDA volume
2 (PPF).
All of the technical requirements included in the delivery specification / drawing must be documented to an
appropriate extent by the supplier in this report.
The first article inspection report includes (depending upon product):
� A completely filled in and signed cover sheet
� A copy of the signed, current HUHN drawings or customer drawings with numbering for all features
included in the delivery specification and, if applicable, the performance specification, in a logical order
� Other specifications and delivery specifications
� Measurement report with all target and actual dimensions
� Material report with all pertinent setpoint and actual values, not older than 1 year
� Function report (qualification results, final measurement reports for electrical parameters)
� Process sequence plan with specification of manufacturing location(s)
� Substantiation regarding manufacturing reliability (process capability, machine capability)
� QM plan / inspection plan
� Materials included in the product
These materials must be declared within the framework of the first article submission process by means
of the IMDS (International Material Data System) (see also http:/www.mdsystem.com).
� Substantiations regarding hazardous materials (CE safety data sheet)
� Deviation approval for non-complying characteristics (must be obtained in advance from HUHN)
If no agreement to the contrary exists, 300 parts must be produced for statistical evaluation of measuring and
test results, of which 25 are actually used. In the case of multi-cavity moulds or several identical tools which
HHR 001, revision level 12/10 Supplier Quality Guidelines Page 7 of 13

are used for the same operation, 100 parts per cavity or tool are required. Reference gauges are to be agreed
upon separately.
The agreed upon first article samples must be shipped to HUHN’s order address along with all required
records in a separate package identified with a coloured label bearing the words “first article samples”.
Shipment of first article samples with incomplete documentation must be approved in advance in writing by
HUHN.
5.1.2 Standard Products
The supplier must submit a first article sample punctually before approval for series production is issued.
After the supplier has submitted parts during the developmental stage, he must initiate component approval
without delay.
The scope of the first article inspection report generally corresponds to the requirements for HUHN-specific
parts, although product-specific simplifications are possible, for example if approvals from our customer have
already been received by the supplier. However, these must be authorised by HUHN prior to first article
submission.
5.2 Approval
HUHN examines the first article inspection report for completeness and compliance with the specified
requirements.
Individual characteristics are double-checked if deemed necessary.
Incomplete test reports, and test reports which exhibit non-approved deviations, are not processed and are
returned to the supplier. This is taken into consideration in the supplier evaluation. If first article submission
has to be repeated through the fault of the supplier, the supplier may be invoiced for processing costs.
HUHN expects first article samples to fulfil all requirements.
If deviations which cannot be corrected on short notice should nevertheless become apparent during the
course of first article production, a written request for limited deviation approval, or a drawing or specification
change, must be submitted prior to first article submission.
The chances of receiving approval must be clarified by the supplier in advance.
Implemented corrections must be approved by resubmitting a new first article inspection report. Agreed upon
correction deadlines must be adhered to.
Component approval is issued by affixing the required signature to the included PSW or VDA cover sheet.
Approved deviations are recorded. The signed cover sheet is returned to the supplier.
The supplier is not authorised to ship series produced parts to HUHN without this approval.
6 Re-Qualification
In order to assure continued quality, the supplier must re-qualify the product/process once a year.
The scope of the re-qualification process must be coordinated with HUHN.
Re-qualification results must be submitted to HUHN of the supplier’s own accord.
If no shipments are received from the supplier for more than a year, the original approval issued by HUHN
expires.
The part must be re-qualified in this case. The supplier must submit a request for re-approval by means of first
article submission (see above).
HHR 001, revision level 12/10 Supplier Quality Guidelines Page 8 of 13

7 Required Duration of Records Retention
The supplier is required to retain all records which substantiate compliance of the components with the
specified characteristics – with respect to specification, manufacturing or testing – for at least 15 years after
delivering the last shipment. This applies to approvals received from HUHN as well.
In the event that HUHN’s customers specify a longer duration for records retention (e.g. ≥20 years), the
supplier is required to adhere to these requirements as well. The requirement for extended records retention is
specified in the Supplier Quality Guidelines, part 2, if applicable.
Refer to VDA volume 1 for details.
HUHN reserves the right to review such records at the supplier’s facility by previous appointment.
Upon request, records must be received by HUHN within 48 hours.
8 Machines and Process Capabilities
All products must be manufactured by means of capable, controlled processes. This must be assured by
means of careful process planning for the product. If no agreement to the contrary exists, for example as
defined in the specifications, the following values apply to all parameters/dimensions:
Short-term process capability: Cmk ≥ 1.67
Preliminary process capability: Ppk ≥ 1.67
Long-term process capability: Cpk ≥ 1.33
These capability values must be agreed upon with HUHN and substantiated for selected
parameters/dimensions within the framework of first article submission.
Corrective measures or other suitable action (e.g. 100% final inspection) must be implemented by the supplier
and approved by HUHN for parameters/dimensions which are below the required capability values, in order to
be able to guarantee that parts meet all specified quality requirements.
9 Traceability
In the event of complaints, the supplier must assure that parts can be traced all the way back to his own subsuppliers
by means of a comprehensive tracing system.
Upon request from HUHN, the supplier must be capable of providing HUHN with the desired information within
a period of 48 hours. The time period may be even shorter in exceptional cases.
10 Environment and Utilised Materials
No hazardous or poisonous materials may be used for the products/processes (composition and
manufacturing) (see VDA list for materials which are subject to mandatory declaration!). Materials which are
subject to mandatory declaration in accordance with this list must be identified in consultation with HUHN.
Further declaration requirements according to HUHN – specifications/drawings and standards are not affected
by such.
All utilised materials must comply with applicable German and European legal requirements (ChemG,
GefStoffV etc.). Details are described in the individual HUHN specifications/drawings and standards.
Only reusable or recyclable materials may be used for packaging, and their composition must comply with
applicable legal requirements.
Packaging for hazardous materials which are contaminated with dangerous residues after use must be taken
back by the supplier, unless an agreement to the contrary has been entered into with HUHN.
Precise instructions for reuse, recycling or disposal must be provided with all materials furnished by the
supplier.
HHR 001, revision level 12/10 Supplier Quality Guidelines Page 9 of 13

Details are established in consultation with HUHN.
The supplier must confirm adherence to this specification as part of the first article submission process.
11 Changes
HUHN must be notified punctually in writing by means of a change request in the event of changes involving:
� Product design and layout
� Manufacturing process
� Utilised materials
� Production location
� Changing sub-suppliers
Changes may not be implemented without written approval from HUHN.
After approval has been issued, changes must be qualified by the supplier. The FMEA, the QM plan
(inspection plan), the part life-cycle etc. must be correspondingly adapted.
First article submission must be completed before parts can be used. The scope of the first article submission
process must be coordinated with HUHN.
Notification indicating positive results of the first article submission process constitutes approval of the
change, and completes the change process.
The first shipment of changed parts must be announced in writing. The shipping documents and the
packaging must clearly indicate initial shipment of changed parts.
12 Shipments
All shipments must be made in accordance with applicable agreements and order releases.
Goods must be identified in a machine-readable fashion, such that traceability is assured.
Products with manufacturing dates which go back more than 12 months may not be shipped to HUHN. If
shipment of such products becomes necessary, the supplier must obtain special approval from HUHN. This
approval must be issued by HUHN in writing. The goods must be separately identified.
Other details shall be established as necessary in the event of approval.
Specially approved materials may not be mixed with other materials/shipments. They must always be shipped
unmixed, in separate containers and with appropriate identification. Any incurred costs may be invoiced to the
supplier.
13 Defective Parts
13.1 At the Supplier’s Facility
Parts which are identified as defective by the supplier, or which presumably do not fulfil the specified
requirements, must be identified immediately and stored such that further processing and shipment to HUHN
is precluded. Delivery of defective parts to HUHN must be prevented.
Measures must be immediately implemented by the supplier in order to inspect previously manufactured parts
and/or lots.
The cause of the defect must be analysed, and must be eliminated by means of suitable process
improvements (e.g. 8D processes).
HHR 001, revision level 12/10 Supplier Quality Guidelines Page 10 of 13

Even if the parts can be rendered usable (fully compliant) by means of rework, rework may only be
commenced after consultation with HUHN. The type of rework to be utilised must be proposed in writing by
the supplier, and approved in writing by HUHN if deemed appropriate. Shipments of rework parts must be
specially identified.
If defective parts have already been shipped to HUHN, HUHN must be notified immediately.
Further measures (e.g. additional tests conducted by HUHN and associated costs) shall be agreed upon
mutually.
13.2 At HUHN’s Facility
If HUHN discovers defective parts in its production line, the supplier shall be notified immediately.
HUHN shall make arrangements with the supplier to return defective parts.
The supplier must analyse all parts returned by HUHN and submit results to HUHN in the form of an 8D
report.
Immediate measures for on-hand inventories and parts allocated to specific orders must be communicated to
HUHN within 24 hours.
If no special agreement to the contrary has been entered into, analysis results must be submitted to HUHN
within 14 workdays.
If processing has not been completed by this deadline, the supplier is required to inform HUHN in writing
regarding the results of ongoing examinations on a regular basis (once a week).
8D processes are not deemed complete until approval has been issued by HUHN.
Implemented corrective measures must be documented.
If the defective parts cannot be returned (e.g. due to an impending production stoppage at HUHN or one of
HUHN’s customers), the parts must be sorted by the supplier at HUHN’s facility. If this is not possible (e.g.
night shift), HUHN shall sort, and if necessary rework the defective parts, at the expense of the supplier after
consulting with the supplier.
13.3 At the Facility of one of HUHN’s Customers
If, during the course of processing a customer complaint, HUHN determines that the problem in question has
been caused by a supplier, the supplier shall be notified immediately.
HUHN shall return all defective parts to the supplier, is as far as no agreement to the contrary has been
entered into.
The supplier must immediately analyse all parts returned by HUHN and submit results to HUHN in the form of
an 8D report. An initial statement must be issued within 24 hours of receipt of the defective parts, and must
above all include preliminary remedial measures (containment action). Processing time allowed until issuance
of the final report shall be specified as a deadline in the complaint. If no special agreement to the contrary has
been entered into, analysis results must be submitted to HUHN within 14 workdays. If processing cannot been
completed by this deadline, the supplier must inform HUHN in writing regarding the results of ongoing
examinations on a regular basis (once a week).
Goal: Complete the entire process within one month.
8D processes are not deemed complete until approval has been issued by HUHN.
Implemented corrective measures must be documented. HUHN shall examine implemented corrective
measures on-site.
In exceptional cases, this duration may be significantly reduced (e.g. 3 days).
HHR 001, revision level 12/10 Supplier Quality Guidelines Page 11 of 13

14 Ongoing Measures During Series Production
The supplier bears full responsibility for the quality of his products.
Amongst other measures, this must be assured by the supplier by means of:
� Process capability analyses
� Process control measures
� Employee training
� Internal audits
15 Mandatory Insurance
The supplier is required to procure insurance coverage for product liability, recall actions and guarantee claims, and
must uninterruptedly maintain such insurance coverage during the entire term of this agreement, and provide
HUHN with substantiation of such insurance coverage at any time upon request.
HUHN shall be granted access to production areas at any time if it becomes necessary in dealing with problems.
Insured sums are based upon the supplier’s risk analysis for his products and processes.
16 Secrecy
Both parties to this agreement undertake to maintain secrecy regarding all information received from the other
party, and to use it exclusively in the interest of the contractual relationship which exists between the parties to this
agreement.
17 Use of Sub-Suppliers
If applicable, the supplier shall bind his sub-suppliers to all requirements specified by HUHN.
HUHN reserves the right to visit such sub-suppliers, in order to gather information regarding their stages of
development, manufacturing processes etc.
This may also involve auditing sub-suppliers in cooperation with, and in the presence of the supplier.
18 Additional Freight Charges
Additional freight charges paid by the supplier must be recorded by the supplier and made available to HUHN for
review upon request.
19 Term of Validity
These supplier quality guidelines are valid indefinitely. They can be terminated by giving three months written
notice.
20 Terms and Conditions of Purchase
HUHN’s current terms and conditions of purchase are an integral part of all purchase orders.
Our current terms and conditions of purchase are available on www.heinrich-huhn.de.
HHR 001, revision level 12/10 Supplier Quality Guidelines Page 12 of 13

21 Revisions
Date of
change:
5/14/2004 3.1 Audits
Section changed: Change:
5.1.1 HUHN-Specific
Components
18 Term of Validity
19 Terms and Conditions
of Purchase
In the case of suppliers who are not yet certified in accordance with DIN EN ISO 9001, VDA
6.1, QS-9000 or ISO TS 16949, or who are unable to substantiate a successfully completed
audit conducted by an automobile manufacturer or a renowned system supplier, HUHN will
conduct an examination or potential analysis if applicable regarding the status of HUHN’s
requirements with respect to the supplier’s quality management system (supplier audit).
Unless otherwise specified, submission of the first article inspection report must be made in
accordance with respectively valid stipulations per QS-9000-PPAP (production part approval
process), level 3, or VDA volume 2 (PPF).
Inserted an additional section entitled “Additional Freight Charges”:
Additional freight charges paid by the supplier must be recorded by the supplier and made
available to HUHN for review upon request.
Replaced by the section entitled “Term of Validity”;
section 19, “Terms and Conditions of Purchase”, becomes section 20 as a result of the altered
sequence.
6/25/2004 1.0 / 1.1 Scope Added HUHNPressTech location (including logo on cover sheet)
7/23/2004
12/02/2010
22 Information
21 Revisions Added “Revisions” as section 21
8 Maschine + Process
Capabilities
2 Quality and
Environmental
Management System
Requirements
The reference "with on one side limited characteristics is" the zero"distant limit to begin" was
removed.
CQI 09-15 requirements added.
3.1 Audits Text partly changed.
20 Terms and Conditions Added: "Our current terms and conditions of purchase are available on www.heinrich-
of Purchase
huhn.de."
22 Information Completely added
Visit the following homepages for support or assistance:
www.vda.de VDA Information (German/English)
www.ts16949.com ISO/TS 16949 Information (English)
www.vda-qmc.de Information VDA and IATF (German)
www.aiag.org ISO/TS 16949 – Information (English)
www.fiev.fr FIEV Information (Französische Automobilhersteller) (French)
www.anfia.it ANFIA Information (Italien/English)
www.smmt.co.uk SMMT Information (English)
www.jedec.com Semiconductor Industry (English)
www.ipc.org Electronics Industries (English)
www.mdsystem.com International Material Data System (German/English)
www.emas-logo.de Eco-Management and Audit Scheme (German)
http://europa.eu.int/comm/environment/emas/index_en.htm
European commission offical EMAS site (English)
HHR 001, revision level 12/10 Supplier Quality Guidelines Page 13 of 13