Ref 01 - SUPPLIER QUALITY AGREEMENT

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SUPPLIER QUALITY AGREEMENT (CF06028 rev 3)
SUPPLIER NAME / LOCATION (TOWN & COUNTRY) Doc ID :
Remove the word Template from this agreement before filling out, and be sure to remove and replace the green
text with the necessary information and make the text black and delete the sections not being used in this
agreement.
Supplier Name: Doing Business As: Date:
Supplier #(s): Address: City:
State / Postal Code: Country: Implantable (Y/N):
Zimmer Biomet Contact and Title: Email Address: Telephone Number:
Supplier Contact and Title: Email Address: Telephone Number:
NOTE: This agreement is applicable for all Zimmer Biomet sites doing business with the supplier.
1. Background
In order to maintain the quality and regulatory compliance of all of its products and/or services, Zimmer Inc.,
Biomet, Inc., its affiliates and subsidiaries (“Purchaser”) has determined it necessary to require each of its
Suppliers to maintain certain quality assurance standards as provided herein.
2. Quality Systems and other applicable regulations and standards

Supplier will comply with the regulation- as far as applicable for Supplier for the respective product - of the current
version of the Council Directive 93/42/EEC of 14 June 1993 concerning medical devices (the “MDD”) and of the
current version of the Medical Device Regulation (EU) 2017/745 (the “MDR”), as applicable in each case. Supplier
shall help Purchaser to comply with these laws in any way possible, in particular by providing information and by
cooperating with Purchaser (e.g. regarding information and other requests by authorities). In addition, Supplier shall
comply and has complied with all laws, regulations and orders of all manufacture, import, export and safe of the
end products. Supplier will maintain a compliant Quality Management Systems based on the product or service
provided (e.g. 21 CFR Part 820, 21 CFR 58, 21 CFR 1271, ISO 17025, ISO 13485, or ISO 9001). The Supplier
quality system review is part of the initial and ongoing assessments performed by Purchaser. Changes from an
existing quality system pertaining to registration/certification and the supplied product or service will require the
Supplier to notify the relevant Purchaser Contact Person in writing prior to the implementation of the change.
Exhibit A gives guidance on supplier changes and will not be considered all-inclusive. External manufacturers of
finished goods and contract labs will be registered and listed its products with the FDA and/or hold certification from
an internationally known organization.
Supplier will make available their ISO or relevant certifications with any updates or re-certifications.
ZBV-AQF-FOR-022-08 based on CF06028 rev. 3 Ref : CP06017 Supplier Quality Agreement (ZBV-AQF-PGE-004)
Ce document est géré informatiquement au sein du SMQ. Le document imprimé est considéré comme une COPIE NON CONTRÔLÉE. Page 1 sur 9
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All applicable elements of a quality system are considered when Purchaser is making its determination whether a
quality system is acceptable, including, but not limited to the following:
• Properly implemented quality procedures for production processing, including validation.
• Appropriate statistical techniques to analyze quality data and production effectiveness.
• Corrective and preventive action system with evidence that actions are effective in preventing and eliminating
defects. These actions will be part of a continuous improvement action.
3. Audits
The Supplier will permit Purchaser, or its designee, to audit the Supplier’s quality system upon receipt of written,
advance notification.
• Supplier will be available to participate in quality assurance meetings at the Supplier’s facility or at Purchaser
to review and update the status of issues pertaining to product or process quality and reliability for the
processes, services and/or products purchased by Purchaser.
• Supplier will grant all relevant Regulatory Agencies i.e. FDA, and ISO Notified Bodies, to whom Purchaser is
accountable, access to its works, to audit the Supplier’s facility and/or records, with or without issuance of
advanced notification by the aforementioned organizations.
o Supplier will notify Purchaser, via written correspondence to their Purchaser Contact, of any regulatory
body i.e. FDA (FDA, competent authority or other regulating bodies) of an inspection that is scheduled or
initiated at their facility.
o Supplier will provide required details of any actions (e.g. correction, removal, FDA 483 or other regulatory
inspection findings, any warning letter issued by FDA, etc.) that impact the products and/or services the
Supplier provides to Purchaser.
• Unannounced audit expectations: (Delete if not considered a Critical Subcontractor)
o Supplier will permit unannounced audits with the caveat that require visitor screening, escorts, and
recognition that total access may not be granted per the company's Technology Transfer Control Plan (or
other procedural) requirements due to International Traffic in Arms Regulations (USA - ITAR 22 CFR
120-130 ) regulations.
o The Supplier agrees to include in their Quality Management System, a procedure explaining the
expectations of unannounced audits to include, but not limited to the following:
 Immediate notification to responsible Purchaser representative via phone.
 Notification of notified body of production windows and changes.
 Coordination with Purchaser before and after the audit when Purchaser product is in scope of the
audit.
 Training of staff regarding responsibilities and requirements during unannounced audits.
4. Acceptance Activities Quality Records/Retention

Acceptance activities required by Purchaser for any particular finished goods or service via requirements that are
contained in purchase specifications from Purchaser: included in or applicable to a purchase order, Statement of
Work (SOW or contract) and Product Specifications, the Supplier will:
• Include in their Device History Record (DHR) documented inspected, tested, or otherwise product verification
as conforming to Purchaser specified requirements.
• Include acceptance activity records of appropriate test/inspection criteria, validation records, revision level of
documents/equipment/software used, operating procedures (planning, routing or traveler sheets), dates of
test/inspection, and the results.
• Ensure records are stored in a manner to prevent mix-ups, along with stored in a manner to minimize
deterioration and to prevent loss. Also, this would include electronic records.
• Retain records either onsite or through other means (including electronic or off-site storage) for a period of time
equivalent to the expected life of the device, but in no case less than 15 years from the release date for
commercial distribution of the product, but in no case less than 15 years from delivery of the product to
Purchaser. Any electronic or off-site storage will be easily retrieved within at least 1 day from Purchaser’s
request.
• Notify immediately via written correspondence to the Purchaser Contact Person prior to disposing of any
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records whether this is due to:

o fulfillment of holding period
o Cessation of business with Purchaser and provide notification of closing its facility, and supply (at the
Purchaser’s request) all requested manufacturing and quality related documents.
• Grant access to all manufacturing and quality records by Purchaser employees, agents, contractors and
assigned either directly or by a third party within 2 working days of notice from Purchaser.
o In certain instances (i.e. FDA investigations/inspections), these records may be required to be made
available on the same day or within 24 hours of notice from Purchaser.
• Support Zimmer Biomet regarding technical documentation as defined in the MDD or MDR (as applicable),
including but not limited to the results and critical analyses of all verifications and validation tests undertaken by
the supplier on the Purchaser’s product that demonstrates conformity of the product and services provided.
5. Compliance
Supplier will comply with all Purchaser specifications, including any industry standards such as ASTM, product
listings or applicable print specifications, and any Purchaser quality program for supplier’s (e.g. Supplier
Certification, Skip Lot, or DTS) or requirements applicable to Supplier as Purchaser may develop. Purchaser
reserves the right to amend and modify its supplier quality programs at any time without prior notice.
The Supplier will furnish a Certificate of Conformance (C of C) and/or a Certificate of Analysis (COA) with each
product lot/shipment attesting to the conformance of the product to Purchaser Purchase Order (P.O.)/contract
specifications, drawings and acceptance requirements and/or other Purchaser product requirements, as applicable
to Purchaser.
Supplier will conform to the latest RoHS , REACH, and conflict materials restrictive substances as defined by
United States Dodd-Frank Consumer Protection Act compliance standards and certify that the products provided to
Purchaser, whether component, raw material, or finish good.
Per Medical Device Regulation (Regulation (EU) 2017/746 comply with Restricted Materials/Substances that are
part of the Candidate list of Substance of Very High Concern (SVHC, REACH, Article 59 (10)) will be declared. This
restriction also applies to all carcinogenic, mutagenic and/or reprotoxic substances (CMR) of category 1.A and 1.B,
and, endocrine disruptors (ED) substances with serious effects to human health
Supplier will comply with the new Medical Devices Regulation (Regulation (EU) 2017/745) and certify that the
products provided to Zimmer Biomet whether component, raw material, or finished goods, will integrate the
requirements described in the Article 10.4 of the MDR (Annex I, General Safety and Performance Requirements).
The Supplier agrees to manufacture the Products in compliance with the EU Directive 722-2012 Animal Tissue
used in the manufacture of medical devices or use of material of animal origin.
The Supplier agrees to comply with FDA regulation 21 CFR 801.437; Subpart H--Special Requirements for Specific
Devices, Section 801.437 User labeling for devices that contain natural rubber. This section applies to all devices
composed of or containing, or having packaging or components that are composed of, or contain, natural rubber
that contacts humans. The term "natural rubber" includes natural rubber latex, dry natural rubber, and synthetic
latex or synthetic rubber that contains natural rubber in its formulation.
6. Adverse Non-Conformance Product Event

Supplier will implement and maintain a documented system to quarantine, and report to Purchaser any product
issue that may compromise the safety of the product user or diminish the quality of the product thereby warranting,
ceasing continued shipment of the product or requiring a product recall.
• If Supplier becomes aware of any product complaints or adverse reactions that impact the products and/or
services which are sourced by the Purchaser, the Supplier will immediately notify their Purchaser Customer
Service team at 1-800-348-2759 or submit the complaint electronically to the Purchaser via Purchaser
Product Experience Reporting (PER) process at [email protected].
• The Supplier, if requested by Purchaser, will conduct internal investigations, record reviews, and sample
evaluations as required to determine the validity of the complaint. The findings from the investigation will be
reported to the Purchaser Contact Person within 5 working days of notice from Purchaser or within the
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designated timeframe given by Purchaser.

• In the event Purchaser is required or voluntarily decides to recall or withdraw Product implicating a Supplier’s
processes as potential root cause, the Supplier will fully cooperate with Purchaser in connection with such a
recall or withdrawal.
• Zimmer Biomet will be solely responsible for the reporting of adverse experiences with respect to the Product to
the FDA and other global Regulating Bodies. Zimmer Biomet will be responsible for disposing of any recalled
or withdrawn Product.
7. Supplier Corrective Action

Upon notice from Purchaser of any deficiency in supplier’s quality system, product or service, the Supplier will
provide documented corrective action(s) to prevent future deviations from the specification or quality system
requirement.
• Upon Purchaser request, the Supplier will provide to the Purchaser’s Supplier Quality team the established
SCAR document and all supporting documents pertaining to the specific problem/defect description (including
similar product), containment actions performed, and initial investigation performed. All documentation and
actions performed will be provided within the required time necessary by the Purchaser’s compliance system,
which is ten (10) calendar days, or less if there is an impact to the Purchaser’s supplied material or service.
• The Supplier will provide Purchaser; within the Supplier Quality established SCAR documented timeframe, the
root cause analysis, and corrective/preventive action(s) taken to minimize any risk to the Purchaser and
Purchaser’s customers or end users of the product/service furnished by the Supplier.
8. Change Notification
The Supplier will provide written notification to the Purchaser of any changes referenced in Exhibit A and/or in the
Supplier’s quality system immediately using CP06013 Supplier Change Notification Template. This notification will
be submitted in order for the Purchaser to evaluate the impact of the change to the quality of the finished
product/service. See Exhibit A for a list of requirements on changes, which may require advance notification to
Purchaser. This list may not be considered all-inclusive
• Purchaser respectfully requests a minimum of 120-day notice to ensure appropriate reviews can be
completed, including any Regulatory evaluations.
• Supplier changes will be approved by Purchaser before the Supplier implements the change.
• Any impact to open Purchase Orders which are due to the change will be communicated to the Purchaser’s
Sourcing team in order to assess the impact on deliveries to the Purchaser.
• Any changes requested by the Supplier or by the Purchaser that may affect the supplier risk classification for
the product/service they provide, will require an evaluation of the Supplier Quality Agreement to determine if the
change impacts an existing Agreement. If changes are necessary a new Agreement will be initiated by the
Purchaser to the Supplier
• The Supplier will notify the Purchaser of changes in the Supplier’s Management structure via written
correspondence, which may be in the form of a letter or electronic means.
o Such changes includes, but are not limited to, changes in management with executive responsibility or
changes in management responsible for regulatory, quality or quality systems.
9. Production/Process Controls
Supplier will ensure that all processes that directly affecting the quality of products and/or rendered services, are
clearly defined and conforming to Purchaser purchasing specification requirements applicable to Purchaser.
Supplier’s process controls will include, but not limited to:
• Documented procedures defining the manner in which processes are to be performed and measured.
• Use of suitable equipment and environment to produce products or services.
• Monitoring and controlling of critical process parameters and product characteristics using in-process
inspection and where appropriate, supporting with statistical methods. The evaluation of the produced
products/rendered services will be performed per Purchaser established critical to quality (CTQ) dimensional
requirements as signified through patient risk criticality.
• Supplier will be required to demonstrate risk mitigation of process risk per ISO 14971 (i.e., pFMEA (Process
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Failure Mode Effect Analysis), or relevant risk management tools).

• Documented changes to production and process controls.
• Trained qualified personnel to perform operations on Purchaser products and/or executed services. For
example, where certifications are required (i.e., Fluorescent Penetrant Inspection (FPI), X-Ray, welding, etc.)
only certified operators are to perform these operations.
• Defined and controlled criteria for workmanship standards.
• System(s) to protect Purchaser’s products from contamination by unapproved foreign materials.
10. Identification & Traceability

Supplier shall identify the product by suitable means throughout product realization and shall establish documented
procedures for such product identification
Supplier shall ensure the traceability of the batches manufacture and establish documented procedures for
traceability. Such procedure shall define the extent of product traceability and the records required.
A batch is defined as having resulted from the same process and undergone the same processes and treatments in
the same period, for the same product reference and for a two raw materials batches.
11. Process Validation

For Supplier’s processes or outsourced sub-processes that cannot be fully verified by subsequent inspection or test
methods (e.g. Welding, brazing, heat treating, passivation, or anodizing), the Supplier, and their sub-tier supplier(s),
will have an established validation process that meets the needs of the specified quality system, and will minimally
consist of Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), and 21
CFR Part 11 compliance when applicable. Supplier’s validation process will include:
• Appropriate statistical rationale for sampling strategy.
• Definition of equipment and process parameter requirements of validation IQ/OQ/PQ.
• A post-validation monitoring and control process defined by the Supplier and agreed upon by Purchaser.
• A process for evaluating changes against the current validated state of the process and a method detailing
revalidation activities when required.
• The Supplier agreeing to notify Purchaser immediately if any validation process deviations occur. The
Supplier will evaluate and analyze the deviation where appropriate, and provide the results to Purchaser for
consideration for acceptance.
• A method, if requested, to provide validation protocols and results of pre-validation process development
activities including any changes to processes or equipment for which the validation requirements have been
established and mutually agreed upon.
12. Implantable Titanium Raw Material (Delete if site is not governed under current procedure for
process)
The Supplier will only source titanium used in the Purchaser’s implantable devices, from the Purchaser’s defined
Implantable Raw Material Approved Supplier List (ASL) or implantable materials referenced to that site as
specified. This requirement will be forwarded to any of the Purchaser’s Supplier’s.
13. Supplier Sub-tier Contractors

Purchaser may require documented proof that the Supplier has ensured the effectiveness and adequacy of its sub-
tier contractor controls. Upon such requirement, the Supplier will promptly furnish such documentation requested
by Purchaser of its subcontractor’s controls. The Supplier will ensure that subcontractors comply with all
documented agreements including as a minimum:
• Methods for monitoring the subcontractor.
• Stipulations for obtaining from each subcontractor a duly signed and authorized written agreement, in which the
subcontractor explicitly confirms its compliance with Purchaser purchasing specifications, including supplier
change notification.
• Provisions of such agreement to Purchaser.
• Provisions for submission of any and all additional documentation to Purchaser, including but not limited to
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process validation documentation.

• Suppliers and sub-contractors are not to knowingly work with distressed nations or nations that promote child
labor.
14. Packaging and Shipping Methods

Supplier will, as deemed appropriate by Purchaser, implement and follow packaging, shipping methods necessary
to prevent cosmetic, mechanical and electrical damage to the products shipped, as applicable. The Supplier will
package the product as specified on the part drawing. If no packaging is specified on the part drawing, the Supplier
will package the product so as to prevent damage or deterioration of the product and labels during shipment per
Purchaser specified requirements.
15. Product Registration

Upon a Purchaser representative request, the Supplier will submit all non-proprietary information needed for
registration of the product. The Supplier will ensure that Purchaser is involved in any changes, which may affect
the Product’s regulatory status. The Supplier will make available proprietary information to regulatory agencies
through a master file or equivalent document in the English language.
16. Term
This Agreement will remain in effect from the date of the last signature affixed below and will continue until
Purchaser determines a new agreement is necessary.
17. Miscellaneous
This Agreement is the complete, final and exclusive understanding of the parties as to the matters covered herein
and supersedes any and all prior Supplier Quality Agreements. Notwithstanding the foregoing, this Agreement
does not supersede or replace any separately negotiated quality agreement. To the extent that a conflict arises
between this Agreement and a 3rd Party Agreement with more specific Quality and Regulatory terms, the 3rd Party
Agreement supersedes all.
No amendment, modification or supplement of any provision of this Agreement will be valid or effective unless
made in writing and signed by a duly authorized management representatives of each party. Neither party will have
the right to assign any of its rights or obligations under this Agreement without the prior written consent of the other
party.
No provision of this Agreement will be waived by any act, omission or knowledge of a party, its agents or
employees.
This Agreement will be governed by and interpreted in accordance with the laws of the (State of XXX),
United States of America or (Country of XXX), without regard to its choice of law rules.
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By signing below, the Supplier and Purchaser agree to the terms hereof and the Supplier agrees to meet all
requirements that apply for any and all products and services provided by the Supplier to Purchaser.
Supplier’s Quality Management Supplier’s Operations Management
Printed Name Printed Name
Title Title
Date Date
Signature Signature
Zimmer Biomet Supplier Quality Management Zimmer Biomet Sourcing Management

Printed Name Printed Name
Title Title
Date Date
Signature Signature
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Exhibit A
Type of Change or Activity*
Packaging Manufacturer or
Non-Implants, Instruments
Sterilization, Microbiology
Contractors Consultants,
Special and/or Validated
Engineering Services,
Implants and Implant
Fixture-Gage, Test-
Raw Material, Mfg.
Packaging Service
Calibration, NDT
Components
Processes**
Distributors
Material
I) Production Facility
X X X X X X X X
Create new building, change buildings or move product to another location.
II) Equipment
Change type of equipment
X X X X X X X
Move to different equipment same technology, i.e. brand of equipment, Lathe to
screw machine, manual to CNC, Change fume hood, etc.
Change to specific equipment with similar capabilities
Move from Sealing machine serial number 123 to sealing machine serial number X X X X X X
456; change in NDT equipment.
Movement of equipment within a facility – that affects a validation. X X X X X X
Change/reduced frequency or method of Preventative Maintenance. X X
Change to Non-routine maintenance. X X
Change machine or tooling design. X X X X X
Change machine program. X X X X
Change process parameters. X X X X X X
Packaging Materials or Packaging processing X X X X X X
Change featuring materials that come into contact with the product. X X X X X
III) Subcontractor Change
Move product, process, or service from in-house to subcontractor, Subcontractor to X X X X X X X X
in-house, or from subcontractor A to subcontractor B.
IV) Change Inspection Requirements
All changes in inspection method, frequency, sampling methods, etc.
Note: changes that increase frequency or increase detect-ability, i.e. the use of X X X X X X X
equipment with higher accuracy and precision may be implemented with notification
to Purchaser to follow.
V) Manufacturing Materials
Change Manufacturing Materials that come in contact with the Product X X X X X X X
coolant, machine lubricants, polishing compound, cleaning solutions, etc.
VI) Manufacturing process flow
X X X X X X
re-sequencing, changes to established router, additions/deletions, etc.
VII) Rework and/or Reprocessing not outlined on the original approved
Control Plan or Specification
X X X X X X X X
A loop added to route product back to a previous step for the purpose of repeating
work done to bring product into specification.
VIII) Forming Operations
Casting, forging, wrought operations as related to metals (e.g., changing
X X X X X
configurations, release agents, mold, or die materials are reportable changes) and
compression molding, ram extrusion, or injection molding as related to polymers.
IX) Raw Material
Change in formulation, purity, or strength (Including additives and percentages). X X X X X
X) Management Change
Change in the Organizational Management structure. These changes include, but
X X X X X X X X
are not limited to, changes in management with executive responsibility, or
changes in management responsible for the regulatory, quality or quality systems.
XI) Design Changes
Design or design drawing changes that affect Zimmer Biomet product X X X X X X X X
XII) Software Change
Changes in a software application that would affect a Zimmer Biomet product,
X X X X X X X X
product drawing or service. This would include software as an application for a
medical device.
XIII) QMS Change
All changes on the ISO certificate. These could include a change on the scope or X X X X X X X X
the loss of the certificate.
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* Exhibit A is a guide for reporting requirements for process and material changes and is not intended to be all inclusive.**Applies to processes
where the results of the process cannot be fully verified by subsequent inspection and test. The process is to be validated with a high degree of
assurance and approved according to established procedures.
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ZimmerBiomet France revision history

N° de CAPA, NC, ou
Change Control
Indice Date Nature de la modification associé.
/Index /Date /Nature of the modification / N° of CAPA, NC, or
Change Control
associated.
En accord avec la procédure Maitrise de la documentation 05-001/ZBV-SMQ-
PGE-009 il a été réalisé les modifications suivantes :
 Modification de la codification du document ainsi que de l’ensemble
des références documentaires dans le corps du texte,
 Changement de la page de garde,
 Aucune modification du fond,
 Le changement de codification n’entraine pas de révision de l’indice
qui est conservé.
CAPA : CA-003324
21 Mars
07 20178
Change Control : 2017-
According to the Documentation Mastering procedure 05-001/ZBV-SMQ-PGE- 0204
009, the following modifications have been made :
- Modification of the codification of the document as well as all the
documentary references in the body of the text,
- Changing the cover page,
- No substantial change,
- The codification change does not affect the index which is
maintained.
Integration of CF 06028 rev 3:

30 July On chapter 2- Quality systems: Add regulation MDD & MDR
08 CC2019 -0236
2019 On Chapter 4 – Acceptance Activities : Add technical support
regarding MDR & MDD
14 Nov Add in the Exhibit A : part XIII) QMS Change.

09 CC2019 -0236
2019
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Corporate REVISION HISTORY CF06028:

Rev Revised by Date Released Description of Change
1 Doug Calvelage See DC New release into Zimmer Biomet Corporate document template.
System Template is a combined document with legacy Zimmer global
procedure ZMH-QMS-4-014 and Biomet template CF0604 for
best practice.
2 Doug Calvelage See DC • Added instructions at top of page in green, to note as
System “Remove the word Template from this agreement before filling
out, and be sure to replace the green text with the necessary
information and make the text black and delete the sections
not being used in this agreement”.
• Updated the information section requirements on the
beginning of page one.
• Added “NOTE: This agreement is applicable for all Zimmer
Biomet sites doing business with the supplier.
• Added “Make Available Their” and removed “Submit Updated”
verbiage in the ISO line of Quality Systems section
• Added the verbiage “Remove the word Template from this
agreement before filling out, and be sure to remove ALL
green text and any sections not being used in this agreement”
in the unannounced audit information.
• Added the word “knowingly” in the last bullet of the Supplier
Sub-Tier Contractor Section
• Added 2 new line items in Appendix A
XI) Design Changes
Design or design drawing change to product supplied to Zimmer
Biomet
XII) Software Change
Changes in a software application that would affect a Zimmer
Biomet product, product drawing or service. This would include
software as an application for a medical device.
• Changes requested from Sourcing peer review 9/12/17
Added table for agreement information at beginning of document
to include the applicable information
Added information to reference CP06018 Corporate Supplier
Quality Guidebook on page one
Capitalized Supplier throughout where the verbiage is possessive
Updated verbiage in bullet points of Acceptance Activities Quality
Records/Retention section
Updated verbiage in first paragraph of Compliance section
Updated verbiage in first and section bullets of Supplier
Corrective Action section
Updated verbiage in first paragraph of Change Notification
section
Updated verbiage in bullet points of Change Notification section,
along with removing redundant bullets
Updated verbiage in Implantable Titanium Raw Material and
Supplier Sub-Tier Contractors section
3 •

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Supplier #(s): Address: City:

State / Postal Code: Country: Implantable (Y/N):

Zimmer Biomet Contact and Title: Email Address: Telephone Number:

Supplier Contact and Title: Email Address: Telephone Number:

2. Quality Systems and other applicable regulations and standards

4. Acceptance Activities Quality Records/Retention

records whether this is due to:

6. Adverse Non-Conformance Product Event

designated timeframe given by Purchaser.

7. Supplier Corrective Action

Failure Mode Effect Analysis), or relevant risk management tools).

10. Identification & Traceability

11. Process Validation

13. Supplier Sub-tier Contractors

process validation documentation.

14. Packaging and Shipping Methods

15. Product Registration

Supplier’s Quality Management Supplier’s Operations Management

Printed Name Printed Name

Zimmer Biomet Supplier Quality Management Zimmer Biomet Sourcing Management

ZimmerBiomet France revision history

Integration of CF 06028 rev 3:

14 Nov Add in the Exhibit A : part XIII) QMS Change.

Corporate REVISION HISTORY CF06028:

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