Attachment A Purchased Material Quality Terms
Exhibit 10.17
STRATEGIC SUPPLIER ALLIANCE AGREEMENT CONTRACT MANUFACTURING EMEA
GE HEALTHCARE
GE Healthcare entity (GEHC) | Other Party (the Supplier) | |
GE Healthcare Bio-Sciences AB | Repligen Corporation | |
Address | Address | |
Björkgatan 30, 751 84 Uppsala, Sweden | 41 Seyon Street Building #1 suite 100 | |
Registration number | Waltham, MA 02453 USA | |
556108-1919 | Registration number | |
AGREEMENT | GEHC REF: |
The Parties hereby agree that the following terms and conditions shall apply:
A. | Purpose |
GEHC and the Supplier are entering into this Agreement for the outsourcing by GEHC of the manufacture of the Products by the Supplier. Pursuant to the terms and condition of this Agreement, the Supplier shall manufacture and sell to GEHC, and GEHC shall purchase from the Supplier the Products meeting the specifications referred to in Attachment C (the Products) in such amounts as GEHC may order from time to time on the terms and conditions set out in this Agreement. GEHC shall pay the price of the Products specified in Attachment C (the Prices).
B. | Documents |
The following attachments are an integral part of this Agreement (the Attachments). The provisions of each Attachment shall be incorporated by reference into and deemed to be part of this Agreement. The order of precedence shall be as follows, unless otherwise agreed:
QUALITY & INTEGRITY TERMS
Attachment A - Supplier Quality Requirements
Attachment B - Supplier Integrity Statement
BUSINESS TERMS
Attachment C - Products, Prices, Specifications (if any),
Attachment D - Business Terms
GENERAL TERMS
Attachment E - General Terms and Conditions
TECHNICAL TERMS
Attachment F - GEHC Production Know-How
C. | Term |
Effective Date: 2010-01-01
Agreement Term: This Agreement shall commence on the Effective Date and, subject to the rights of termination in clause 16 of Attachment E, shall continue for a period of five (5) years. The Parties shall negotiate eighteen (18) months prior to the expiration of the Term to decide whether to renew this Agreement.
This Agreement has been duly executed by each of the Parties
Signed for and on behalf of GEHC | Signed for and on behalf of the Supplier | |||||
Signature | /s/ Peter Ehrenheim | Signature | /s/ Walter C. Herlihy | |||
Name (capitals) | PETER EHRENHEIM | Name (capitals) | WALTER C. HERLIHY | |||
Title | President and CEO | Title | President and CEO |
Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Companys application requesting confidential treatment under Rule 24b-2 of the Exchange Act; [*] denotes omissions.
Attachment A
Purchased Material Quality Terms
Supplier Name: Repligen Corporation
Version No.:
The Parties are committed to quality in the performance of this Agreement. Accordingly, all Products shall conform to the Purchased Material Quality Requirements set forth below.
Applicable To All Suppliers:
Section 1 - Quality Systems: The Supplier shall maintain a documented quality system, and the Supplier shall be in compliance with ISO 9001 or equivalent. Key components of a robust quality system are properly implemented quality procedures for collection and processing defects (parts or services), appropriate statistical techniques to analyze defects and identifying opportunities for corrective and preventive actions, along with evidence of validation that actions are effective in eliminating and preventing further defects. Upon request from GE Healthcare, the Supplier shall provide documented corrective action plans to prevent future deviations from the specification within thirty (30) days from receiving a corrective action request from GE Healthcare.
To ensure products and services provided to GE Healthcare shall meet or exceed GE Healthcare requirements, GE Healthcare may audit the Suppliers quality system at periodic intervals upon 30 days written advance notification, to inspect and observe the Suppliers manufacture of Products, to audit the Suppliers quality control and inspection procedures, and to have access to all data and documentation from such control of the Products and to take samples and make such other investigations as GEHC deems necessary. The Supplier shall reserve the right for GEHC to perform such inspections on the premises of subcontractors engaged by the Supplier, such inspections to be scheduled by the Supplier following reasonable prior notice by GEHC and to be carried out jointly by representatives of both Parties and at the sole expense of GEHC. GEHCs right of inspection under this head shall not diminish the Suppliers obligation to deliver Products which comply with the specifications of this Agreement. GE Healthcare may also request periodic, joint quality assurance meetings at the Suppliers facility to discuss and resolve product quality and reliability issues.
Section 2 - Quality Record Retention: If the Supplier is required to perform acceptance activities per GE Healthcare written agreement or purchase specification, the Supplier shall maintain records of the acceptance activities for the services performed and/or products and services delivered to GE Healthcare. These records may include as appropriate test/inspection criteria, revision level of documents/equipment/software used, operating procedures (planning, routing or traveler sheets), dates of test/inspection, and the results. The records required shall be retained until GE Healthcare notifies the Supplier that the product life has ended or for a minimum of ten (10) years, whichever is longer, unless the required records are submitted to GE Healthcare by written agreement or purchase specification.
Section 3 - Compliance: The Supplier shall comply with the terms of the Purchase Order or purchase agreement with GE Healthcare (Agreement). The Supplier shall maintain compliance with any and all laws and government regulations that apply in the manufacturing and delivery of its products or services. Such laws may include, but are not limited to, regulations and directives, labor laws, environmental laws, Custom Trade Partnership Against Terrorism (CTPAT) and product safety laws. The Supplier shall provide GE Healthcare all information requested that is necessary to enable GE Healthcare to comply with the laws and regulations applicable to the GE Healthcare sale and use of GE Healthcare products. As per GE Healthcare
Strategic Supplier Alliance Agreement - GEHC Directs EMEA Contract Manufacturing / Version Supply 1.0 | 2 (30) | |
Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Companys application requesting confidential treatment under Rule 24b-2 of the Exchange Act; [*] denotes omissions. |
purchase specifications or for OEM (Original Equipment Manufacturer) items, the Supplier shall maintain compliance to industry standards and product listings for all Products delivered to GE Healthcare.
Section 4 - Change Notification: Changes proposed by Supplier, both material and process or software changes, which may affect form, fit, function, reliability, serviceability, performance, functional interchangeability, regulatory compliance, safety, options or spare parts interchangeability or interface capability with GE Healthcare Product must be submitted along with a written change notice, for GE Healthcare approval. This includes, but is not limited to, changes of sources of material and parts, changes in manufacturing processes, test procedures, manufacturing locations, relocation or replacement of equipment and any similar changes that are anticipated by Sub-Suppliers. Items affected by such changes may not be delivered to GE Healthcare until the Supplier has received written approval for the changes from GE Healthcare. At minimum, the change notice must include the Suppliers affected part number or software revision, date of implementation, serial number effectivity of the assembly that is changed, reason for the change, specific details of the change and, if available, supporting data that demonstrates that part reliability has not been impacted negatively. The change must not be implemented without prior written consent from GE Healthcare, which shall not be unreasonably withheld. In addition, GE Healthcare has the right to request samples for evaluation prior to approval by GE Healthcare of such changes.
Section 5 - Specifications: The Supplier is responsible to meet or exceed the part requirements and Specifications as referenced in the Agreement. The Supplier is accountable to ensure that delivered items meet the requirements of the revisions and/or versions specified on the applicable Agreement.
The Supplier shall ensure that GE Healthcare documentation is controlled and distributed with the correct revision level to the appropriate personnel that produce the product for GE Healthcare. The Supplier shall also ensure that all GE Healthcare documentation is treated as proprietary and confidential.
For GE Healthcare designed Products, the Supplier is responsible for ensuring that all applicable GE Healthcare documentation is provided to all of the Suppliers Sub-Suppliers involved in the supply of product for GE Healthcare. The Supplier shall ensure that both they and their Sub-Suppliers that use GE Healthcare engineering documentation are maintained in compliance with all accepted Engineering Change Requests/Engineering Change Orders issued by GE Healthcare.
Upon request from GE Healthcare, the Supplier shall ensure that part qualification is conducted and documents are submitted as required. The part qualification requirements shall be determined by GE Healthcare and shall consist of at a minimum a part layout plan, capability study, and a process control plan.
Section 6 - Electrostatic Discharge: IF ELECTROSTATIC DISCHARGE (ESD) SENSITIVE DEVICES ARE SUPPLIED TO GE HEALTHCARE, THE SUPPLIER MUST HAVE AN ACTIVE ESD PROGRAM AND USE PROPER ESD HANDLING AND PACKAGING PROCEDURES. APPLICABLE COMPONENTS INCLUDE CIRCUIT BOARDS, ELECTRONIC ASSEMBLIES WITH EXPOSED COMPONENTS OR CONNECTORS, SEMI-CONDUCTORS AND ANY OTHER DEVICES THAT MAY REQUIRE ESD PROTECTION. SUPPLIERS MUST MAINTAIN RECORDS OF THE TESTING DONE AND TRAINING PROVIDED.
Section 7 - Packaging and Shipping Methods: The Supplier shall provide packaging and shipping methods to prevent cosmetic, mechanical and electrical damage to the Product. The Supplier shall meet or exceed the detailed specifications of the GE Healthcare packaging requirements found in the Specification
Section 8 - Order of Precedence: This attachment A shall be an addendum to the Strategic Supplier Alliance Agreement (SSAA) between Supplier and GE Healthcare. Any conflict between this Attachment A and the other Attachments of the SSAA regarding the minimum material quality requirements shall be resolved pursuant to the latter. Any conflict between this Attachment A and the Purchase Order regarding the minimum material quality requirements shall be resolved pursuant to the terms of this Attachment A.
Strategic Supplier Alliance Agreement - GEHC Directs EMEA Contract Manufacturing / Version Supply 1.0 | 3 (30) | |
Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Companys application requesting confidential treatment under Rule 24b-2 of the Exchange Act; [*] denotes omissions. |
By signing below, you agree to the terms hereof and consent to meet all requirements that apply for any and all products and services provided to GE Healthcare.
Agreed to and Accepted by Supplier | ||
Signature: | /s/ Daniel P. Witt, PhD | |
Printed Name: | Daniel P. Witt, PhD | |
Title: | Vice President, Operations | |
Date: | 2/2/2010 | |
Supplier Name: | Repligen Corporation |
Agreed to and Accepted by the General Electric Company on Behalf of its Division, GE Healthcare
Signature: | /s/ Peter Ehrenheim | |
Printed Name: | Peter Ehrenheim | |
Title: | President and CEO | |
Date: | 1/27/2010 |
Strategic Supplier Alliance Agreement - GEHC Directs EMEA Contract Manufacturing / Version Supply 1.0 | 4 (30) | |
Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Companys application requesting confidential treatment under Rule 24b-2 of the Exchange Act; [*] denotes omissions. |
Attachment B
Supplier Integrity Statement
Supplier Integrity, Business Conduct, and Compliance Requirements
A. | Supplier agrees (a) to comply with all applicable legal, as well as GEHC policy, requirements (including those relating to labor, the environment, health and safety, wages, hours and conditions of employment, occupational safety, discrimination, sexual harassment, immigration, minority owned businesses, intellectual property rights and improper payments); (b) that Supplier is responsible for ensuring that Suppliers employees, contractors, representatives and sub-suppliers understand and comply with the same legal and GEHC policy requirements; and (c) that the requirements referenced in (a) and (b) above include the following: |
(1) | Code of Conduct. Maintain and enforce written company policies requiring high ethical conduct and strict adherence to lawful business practices, including a prohibition against bribery of government officials. |
(2) | Labor Matters. |
(i) | Employ only workers above the applicable minimum age requirement or the age of 16 whichever is higher. |
(ii) | No use of forced, prison or indentured labor, workers subject to any form of compulsion or coercion, or labor in violation of minimum wage, hour of service, or overtime laws in the country of manufacture, and prohibit physical, sexual or psychological harassment or coercion. |
(iii) | Allow workers to freely choose whether to organize or join associations for the purpose of collective bargaining as provided by local law. |
(iv) | Assure that workers are hired, paid and otherwise subject to terms and conditions of employment based on their ability to do the job, not on the basis of their personal characteristics such as race, national origin, sex, religion, ethnicity, disability, maternity, age, and other characteristics protected by local law; provided, however, that the foregoing does not bar compliance with affirmative preferences that may be required by local law. |
(3) | Environmental Compliance. Comply with all applicable environmental laws and regulations, including: (i) maintaining and enforcing written and comprehensive environmental management programs that are subject to periodic audit by GEHC or its representatives; (ii) continuing compliance with all required environmental permits; and (iii) strictly not negligently permitting any discharge to the environment in violation of law, or that would otherwise have an adverse impact on the environment. |
(4) | Health & Safety. Provide workers with a safe workplace that complies with applicable health and safety standards as well as appropriate living conditions. |
(5) | Improper Payments and Business Dealings. Not offer or provide, directly or indirectly, anything of value (including cash, illegal political contributions, bribes or kickbacks or other improper payments) to any GEHC employee, representative, customer, government official, or other third party in connection with any GEHC procurement, transaction or business dealing. Prohibitions include offering or providing (directly or indirectly): (i) any consulting, employment or similar position to any GEHC employee (or their family member or significant other) involved with a GEHC procurement; (ii) GEHC employees and representatives with any gifts, other than gifts of nominal value to commemorate or recognize a particular GEHC-supplier business transaction or activity; and/or (iii) GEHC employees and/or representatives with the opportunity to participate in any contest, game or promotion. In addition to the foregoing, comply with all applicable laws of the United States and other countries relating to such matters. |
(6) | Business Entertainment of GEHC Employees and Representatives. Comply with the business entertainment (including travel and living) policies established by GEHC and which govern GEHC employees and representatives, including understanding those business entertainment policies of the applicable GEHC component or operation before offering or providing any GEHC employee or representative any form of business entertainment. Never offer to a GEHC employee or representative any form of business entertainment under circumstances that would create the appearance of an impropriety. |
(7) | Collusive Conduct and GEHC Procurements. Comply with all applicable competition laws, including, but not limited to: (i) not engage in prohibited communications or enter into agreements with competitors that can affect competition; (ii) not share or exchange any price, cost or other competitive information, nor engage in any other collusive conduct with any other third party supplier or bidder to GEHC with respect to any proposed, pending or current GEHC procurement; and (iii) avoid even the appearance of improper conduct. |
(8) | Intellectual & Other Property Rights. Respect the intellectual and other property rights of others, including GEHCs. Only use GEHC information and property (including tools, drawings and specifications) for the purpose for which they are expressly provided and for no other purposes. Take all necessary steps to safeguard and maintain the confidentiality of GEHC proprietary information, including maintaining it in confidence, only in secure work areas, and not disclose it to any third parties without the prior written permission of GEHC. Only transmit GEHC information over the Internet on an encrypted basis. Observe and respect all GEHC patents, trademarks, trade secrets, and copyrights, as well as comply with such restrictions or prohibitions on their use as GEHC may from time to time establish. |
(9) | Export and International Trade Controls & Customs Matters. Comply with all applicable import and export control laws and regulations, including those of the United States, and not transfer GEHC technical information to any third party |
Strategic Supplier Alliance Agreement - GEHC Directs EMEA Contract Manufacturing / Version Supply 1.0 | 5 (30) | |
Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Companys application requesting confidential treatment under Rule 24b-2 of the Exchange Act; [*] denotes omissions. |
without the express prior written permission of GEHC. Without limitation to the foregoing: (i) comply with all applicable export controls laws and regulations in the export or re-export of GEHC technical information, including any restrictions on access and use applicable to non-U.S. nationals; (ii) ensure that all invoices and any customs or similar documentation submitted to GEHC or governmental authorities in connection with transactions involving GEHC accurately describe the goods and services provided or delivered and the price thereof; and (iii) not participate in any boycotts or restrictive trade practices prohibited by U.S. laws. Supplier will also obtain all applicable permits and licenses necessary to perform its obligations under this Agreement, and upon GEHCs request, will provide GEHC with copies of such permits and licenses. Where Products contain United States components, Supplier will also provide GEHC with details of the United States content value as a percentage of the Product price upon GEHCs request. Additionally and upon request, Supplier will provide ECCN and Harmonized Tariff numbers assigned to Products. |
(10) | Privacy. With respect to data and personal information (including information of GEHC employees, its customers, suppliers, business partners, and patient health information handled and processed on behalf of its customers) (collectively, PI): (i) comply with all applicable privacy and data protection laws globally, or generally acceptable privacy principles where comprehensive privacy laws are not available; (ii) report any improper use or disclosure of PI, as well as successful security breaches, immediately upon becoming aware; (iii) ensure that any employees, contractors, representatives and sub-suppliers to whom it provides PI and/or access to information systems, agree to the same restrictions and conditions set forth herein; (iv) facilitate audits by making its internal practices, books and records relating to the use and disclosure of PI available to GEHC and government agencies (including, the Secretary of the Department of Health and Human Services) for purposes of determining compliance with applicable laws, rules, and regulations; (v) when requested by GEHC, promptly return or destroy, as well as certify in writing to the return and destruction of, all PI and information in any form that allows access to GEHC information systems, and retain no copies of such PI and information; (vi) safeguard PI upon taking possession or exposure to employees and all third parties; (vii) ensure that formal security management systems are employed that eliminates the risk of PI-related security breaches; and (viii) notify GEHC in writing whenever PI will be exported from jurisdictions with data transfer restrictions, or transfer PI to countries without comprehensive data protections laws. |
(11) | Money Laundering Prevention. Comply with all applicable anti-money laundering laws and regulations and GEHC policies established for money laundering prevention. |
(12) | Prohibition of Use of Sub-Suppliers or Third Parties to Evade Requirements. Not use sub-suppliers or other third parties to evade any applicable legal and/or GEHC policy requirements, including those enumerated above. |
(13) | Security Measures. Supplier warrants and represents that it will review and adopt industry standard security measures which are consistent with accepted programs including the US Customs-Trade Partnership Against Terrorism (C-TPAT), the European Unions Authorized Economic Operator program and other similar programs where applicable. Supplier furthermore agree that it will make reasonable efforts to become a member of C-TPAT, or any similar EU/other organization aimed at strengthening and improving supply chain security, in a timely manner if it is eligible to do so. |
(14) | Country of Origin. In accordance with and as required by applicable trade and customs laws, Supplier will mark each Product, as well as Product packaging, containers, labels, and invoices, with the country of origin for the Product. Supplier will also provide acceptable and auditable documentation that establishes the country of origin for all Products, including, without limitation and as applicable, certifications of origin for Products qualifying for EFTA/EU and other preferential duty provisions, as applicable. Without limitation to the foregoing and in marking the Products, Supplier will comply with the requirements of the custom authorities of the country of receipt. |
GEHC policy requirements, including those enumerated above, are subject to modification by GEHC at any time. Supplier agrees to contact its GEHC representative if Supplier has any questions about the foregoing and/or their application to particular circumstances.
B. | Products provided by Supplier may be subject to environmental, health and safety laws and regulations. As a result, Supplier agrees to the following without limitation: |
(1) | Supplier represents, warrants, certifies and covenants that Supplier shall perform all activities required under this Agreement in compliance with all applicable national, EU, state/provincial and local labor, environmental, health and safety laws and regulations. |
(2) | Supplier represents, warrants, certifies and covenants that each chemical substance constituting or contained in Products sold or otherwise transferred to GEHC hereunder is on the list of chemical substances compiled and published by (a) the Administrator of the Environmental Protection Agency pursuant to the Toxic Substances Control Act (15 USC Section 2601 et seq.) as amended; and (b) the equivalent lists in the other jurisdictions to which GEHC informs Supplier or Supplier knows the Products will likely be shipped to or through; or is exempt from the foregoing lists, in which case Supplier shall provide adequate documentation of the validity of the claimed exemption if so requested by GEHC; |
(3) | Supplier will, when relevant, timely provide GEHC with supporting documentation, including without limitation, (a) the exact weight by weight percentage of any REACH candidate list substance constituting or contained in the Products, (b) all relevant information that GEHC requires to meet the obligations under REACH to communicate safe use to GEHCs customers. |
Strategic Supplier Alliance Agreement - GEHC Directs EMEA Contract Manufacturing / Version Supply 1.0 | 6 (30) | |
Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Companys application requesting confidential treatment under Rule 24b-2 of the Exchange Act; [*] denotes omissions. |
(4) | Supplier represents, warrants, certifies and covenants that none of the Products supplied under this Agreement contain any above limits stated in law: (i) lead, mercury, cadmium, hexavalent chromium, polybrominated biphenyls (PBB), polybrominated diphenyl ethers (PBDE) or any other hazardous substances the use of which is restricted under EU Directive 2002/95/EC (27 January 2003) (RoHS Directive), as amended; (ii) arsenic, asbestos, benzene, polychlorinated biphenyls (PCBs), or carbon tetrachloride; (iii) any chemical restricted under the Montreal Protocol on ozone-depleting substances; or (iv) any other chemical or hazardous material the use of which is restricted in any other jurisdictions to which GEHC informs Supplier or Supplier knows the Products are likely to be shipped to or through, unless GEHC expressly agrees otherwise in writing to Supplier referencing this Agreement and Supplier identifies an applicable exemption from any relevant legal restriction on the inclusion of such chemicals or hazardous materials in the Products sold or transferred to GEHC. Upon GEHCs request and subject to the confidentiality provisions of this Agreement and GEHCs ability to meet its compliance obligations, Supplier will provide GEHC with the chemical composition, including proportions, of any substance, preparation, mixture, alloy or goods supplied under this Agreement and any other relevant information or data regarding the properties, including, without limitation, test data and hazard information. |
(5) | Supplier will use all commercially reasonable efforts to establish and maintain an effective program to ensure that the activities of any suppliers it utilizes to provide any chemicals, substances, goods or services that will be incorporated into the Products supplied under this Agreement will be conducted in conformance with Sections B(1) to B(4) above. |
(6) | With respect to any Products or other materials sold or otherwise transferred to GEHC hereunder, Supplier shall provide all relevant information, including without limitation, safety data sheets in the language and the legally required format of the location to which the Products will be shipped and mandated labeling information, required pursuant to applicable requirements such as: (i) the Occupational Safety and Health Act (OSHA) regulations codified at 29 CFR 1910.1200; or (ii) REACH or EU Directive 67/548/EEC, as amended, if applicable, and (iii) any other applicable law, rule or regulation or any similar requirements in any other jurisdictions to which GEHC informs Supplier that the Products are likely to be shipped. |
(7) | With respect to any Products or other materials sold or otherwise transferred to GEHC hereunder, Supplier shall notify GEHC in writing of the presence of any nanoscale material (defined for these purposes as any substance with at least one dimension of such substance known to be less than 100 nano meters in length). With respect to all such nanoscale materials, Supplier shall provide a description of its legal status in the relevant jurisdiction, and any safety data or other notifications that are appropriate in the EU, US and the relevant jurisdiction. |
AGREED TO AND ACCEPTED BY SUPPLIER | ||
BY: | Daniel P. Witt, PhD | |
TITLE: | Vice President, Operations | |
DATE: | /s/ Daniel P. Witt, PhD 2/2/2010 |
SUPPLIER NAME: | Repligen Corporation |
Strategic Supplier Alliance Agreement - GEHC Directs EMEA Contract Manufacturing / Version Supply 1.0 | 7 (30) | |
Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Companys application requesting confidential treatment under Rule 24b-2 of the Exchange Act; [*] denotes omissions. |
Attachment C
Products, Prices and Specifications
Currency: | USD | |
Delivery term: | FCA Waltham, Massachusetts | |
Revision date: | 22 January 2010 |
A.
Product Name | Zäta | |
GEHC Article number | 28-4048-76 |
Supplier Article Number/unit size
20-2501-00 | [*] | |
20-2501-01 | [*] | |
20-2501-02 | [*] | |
20-2501-03 | [*] | |
20-2501-04 | [*] |
[*] | ||
Lead time (PO): | [*] | |
Lead Times for Safety Stock Replenishment | ||
Requirement | Lead time Zata | |
[*] |
Level of Suppliers Safety Stock
[*] based on the average of the [*] of the then current [*] rolling Forecast distributed by GEHC and the prior [*] by GEHC of each of the Products based on [*].
Shelf life | [*] |
B.
Product Name | rPA | |
GEHC Article number | 30-6000-60 |
Supplier Article Number/unit
20-1501-00 | [*] | |
20-1501-01 | [*] | |
20-1501-02 | [*] | |
20-1501-03 | [*] |
[*]
Lead time (PO): | [*] |
Strategic Supplier Alliance Agreement - GEHC Directs EMEA Contract Manufacturing / Version Supply 1.0 | 8 (30) | |
Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Companys application requesting confidential treatment under Rule 24b-2 of the Exchange Act; [*] denotes omissions. |
Lead Times for Safety Stock Replenishment
Requirement | Lead time rPA | |
[*] |
Level of Suppliers Safety Stock
[*] based on the average of the [*] of the then current [*] rolling forecast distributed by GEHC and the prior [*] by GEHC of each of the Products based on [*].
Shelf life | [*] |
C. General Price Terms
All prices above are per gram and shall be set [*] based on the [*] in each of the [*] for the Products that corresponds to the [*] of each of the Products based on the [*]. The price for each of the Products shall be set on the [*] of each [*] and shall remain fixed for that [*]. Example:
[*]
The prices agreed herein do not include the costs of transportation, packaging, shipping or taxes (including VAT) for the Products and will be paid by GEHC. The costs of packaging will be charged to GEHC by Supplier directly and shall be clearly specified on the invoice.
Additional charges: Unless otherwise agreed in this Agreement the Prices include all costs relating to the supply of the Products and GEHC shall not be obliged to reimburse the Supplier for any additional charges or any other costs relating to the supply of the Products that are not specified herein or otherwise agreed in writing by the Parties.
Strategic Supplier Alliance Agreement - GEHC Directs EMEA Contract Manufacturing / Version Supply 1.0 | 9 (30) | |
Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Companys application requesting confidential treatment under Rule 24b-2 of the Exchange Act; [*] denotes omissions. |
Specifications
| ANALYTICAL SPECIFICATION RAW MATERIAL
30-6000-60 Ed. AG | |||||||
Issued by QA/ A Elb-Jorde | Established by R&D/ J Daicic | Valid from 2008-10-17 | Supersedes 30-6000-60 Ed. AF | Page 1 (2) | ||||
rProtein A Code No: 30-6000-60
| ||||||||
1 Packaging instruction | ||||||||
The package shall be suitable for storage of the material. | ||||||||
2 Terms of transportation | ||||||||
At -18 °C or below | ||||||||
3 Storage conditions | ||||||||
Preserve in a well-closed container at or below -18 °C. | ||||||||
4 Shelf life | ||||||||
Estimated shelf life is [*] from the date of manufacture. Final shelf life is to be decided from stability studies. | ||||||||
5 Other name(s) | ||||||||
rPa GE Healthcare | ||||||||
6 Formula and mass | ||||||||
Theoretical Mr. 34 318 Dalton calculated from amino acid sequence. | ||||||||
7 Description | ||||||||
rProtein A is a recombinant engineered form of Staphylococcus aureus Protein A, produced by fermentation of Escherichia coil. The protein is produced with chemicals and materials of non-animal origin. | ||||||||
The product is supplied as a clear, amber frozen liquid free from particulates. |
70-5043-16 / AB Valid from 2007-01-24
Strategic Supplier Alliance Agreement - GEHC Directs EMEA Contract Manufacturing / Version Supply 1.0 | 10 (30) | |
Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Companys application requesting confidential treatment under Rule 24b-2 of the Exchange Act; [*] denotes omissions. |
| ANALYTICAL SPECIFICATION RAW MATERIAL
30-6000-60 Ed. AG | |||||||
Page 2 (2) | ||||||||
8 Requirements on properties | ||||||||
Characteristic | Tolerance limit | Test method | Remark | |||||
1 Visual examination | [*] | 45-2006-68 | ||||||
2 igG-binding activity: % | [*] | 04-0008-64 | ||||||
3 Purity by size exclusion chromatography: % | [*] | 04-0008-66 | ||||||
4 SDS-PAGE | [*] | 04-0008-65 | ||||||
5 Protein concentration (A275); mg/ml | [*] | QCP-1156 | 1 | |||||
6 Microbial contamination CFU/ml | [*] | M-QCP-1003 | 1 | |||||
7 Endotoxin activity EU/mg rProtein A | [*] | M-QCP-1017 | 1 |
Comment:
1) Supplier method, to be available by the supplier on request from GE Healthcare.
GE and GE monogram are trademarks of General Electric Company. © 1999- 2008 General Electric Company - All rights reserved. GE Healthcare Bio-Sciences AB, a General Electric Company. | 70-5043-16 /AB |
Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Companys application requesting confidential treatment under Rule 24b-2 of the Exchange Act; [*] denotes omissions. |
| ANALYTICAL SPECIFICATION RAW MATERIAL
14-0037-84 Ed. AC
| |||||||
Issued by QA/ A Elb-Jorde | Established by R&D/ J Daicic | Valid from 2008-08-19 | Supersedes 14-0037-84 Ed. AB | Page 1 (2) | ||||
ZätA protein 905 Code No: 28-4048-76
| ||||||||
1 Packaging instruction | ||||||||
The package shall be suitable for storage of the material. | ||||||||
2 Terms of transportation | ||||||||
At or below -18 °C | ||||||||
3 Storage conditions | ||||||||
Preserve in a well-closed container at or below -18 °C. | ||||||||
4 Shelf life | ||||||||
Estimated shelf life is [*] from the date of manufacture. Final shelf life is to be decided from stability studies. | ||||||||
5 Formula and mass | ||||||||
Theoretical Mr: 26 748 Dalton calculated from amino acid sequence. | ||||||||
6 Description | ||||||||
ZätA protein is a recombinant protein produced by a Genetically Modified Organism (GMO) in a fermentation process. The substance is a clear, yellowish frozen liquid free from particulates, supplied in a buffer: 20 mM potassium phosphate 150 mM sodium chloride 2 mM EDTA pH 7.0 | ||||||||
The bulk is to be manufactured according to our Base Method, number 14-0040-44. The protein is produced with chemicals and materials of non-animal origin. |
70-5043-16/AB Valid from 2007-01-24
| ANALYTICAL SPECIFICATION RAW MATERIAL
14-0037-84 ED. AC | |||||||
Page 2 (2) | ||||||||
7 Requirements on properties | ||||||||
Characteristic | Tolerance limit | Test method | Remark | |||||
1 Visual examination | [*] | 45-2006-68 | ||||||
2 IgG-binding activity; % | [*] | 04-0008-64 | ||||||
3 Purity by size exclusion chromatography; % | [*] | 04-0008-66 | ||||||
4 SDS PAGE | [*] | 04-0008-65 | ||||||
5 Quantification; mg/ml | [*] | 04-0013-21 | ||||||
6 Microbial contamination CFU/ml | [*] | M-QCP-1003 | 1 | |||||
7 Endotoxin activity EU/mg ZatA Protein | [*] | M-QCP-1166 | 1 |
Comment:
1) Supplier method, to be available by the supplier on request from GE Healthcare.
GE and GE monogram are trademarks of General Electric Company. © 2006-2008 General Electric Company All rights reserved. GE Health Bio-Sciences AB, a General Electric Company. | 70-5043-16 / AB |
Annual Business Attachment / Performance Goals
The purpose of the performance goals are primarily for the Supplier to plan the operations at the Suppliers site and take preventive initiatives so that the set performance goals can be achieved. The results of the Suppliers performance in below areas should be a part of the business updates between the two Parties. While the performance goals are targets and non-achievement of such goals shall not be considered as material breach of contract the Suppler agrees to use all commercially reasonable efforts to achieve the performance goals.
Performance goals:
1. | Deliveries within Specification, agreed lead times and quantities; performance goal is [*] according to the terms in Attachment C) |
2. | Number of complaint reports sent to the Supplier by GEHC; performance goal is [*] |
3. | Business contingency plan and or Quality audits performed and with the result approved; performance goal is [*]. |
Strategic Supplier Alliance Agreement - GEHC Directs EMEA Contract Manufacturing / Version Supply 1.0 | 14 (30) | |
Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Companys application requesting confidential treatment under Rule 24b-2 of the Exchange Act; [*] denotes omissions. |
Attachment D
Business Terms
1. | Specifications |
The Products to be supplied in accordance with the terms of this Agreement are set forth in Products and Prices, Attachment C. A technical specification in relation to a specific Product is referred to as the Specification as set forth in Attachment C.
2. | Delivery documentation |
With each shipment the Supplier shall deliver the following documents to GEHC:
Certificate of Analysis, Packing slip and the Commercial Invoice.
With each shipment the Supplier shall issue a Shippers Letter of Instructions and an Export Declaration as applicable.
3. | Prices and Payment Terms |
a. | Firm Prices. The Prices of the Products are firm for the Term of this Agreement. |
b. | Taxes. Unless prohibited by law, the Supplier will separately indicate on its Invoice any tax that is required to be imposed on the sale of Products. |
c. | Payment Terms. GEHC shall settle any undisputed invoices arising under this Agreement [*] ([*]) days after receiving an Invoice prepared in accordance with the terms of this Agreement. All sums to be paid by GEHC under this Agreement shall be in the currency specified in Attachment C. Interest for late payments shall not apply to payments that GEHC contests in good faith and shall in no event exceed applicable statutory interest rate. |
d. | Productivity improvement. In the event the Parties have jointly contributed to productivity improvements or cost savings achieved by the Supplier the Parties agree to negotiate in good faith a reasonable price adjustment. Price conditions will be changed only upon mutual agreement. |
e. | Invoicing requirements. The Suppliers Invoices shall contain the GEHC Purchase Order number and other such information as may be required by law or requested from time to time by GEHC. Each cost item shall be specified in the invoice. Invoices shall be addressed to GEHC or the GEHC affiliate who has placed the purchase order with the Supplier. |
f. | GEHC mandated changes. It is recognized and agreed by the Parties that GEHC mandated changes in the manufacturing process, quality requirements or standard or in the components and materials used in the process or any other changes in the requirements for the Products may result in an increase in the cost of the Products. The Parties agree to negotiate in good faith to adjust the prices accordingly, provided that the Supplier notifies GEHC in writing of any possible cost increases in advance of the initiation of any such changes. |
4. | Components and Materials |
At GEHCs option, GEHC may instruct the Supplier to procure or provide all materials and components necessary for the manufacture of the Products from an approved supplier, in which case an approved suppliers list shall be maintained by the Supplier. GEHC confirms its approval of the currently used suppliers as notified to GEHC in approved raw material specifications. Any new suppliers selected by the Supplier in connection with the Agreement must be approved by GEHC, whereupon they may be
Strategic Supplier Alliance Agreement - GEHC Directs EMEA Contract Manufacturing / Version Supply 1.0 | 15 (30) | |
Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Companys application requesting confidential treatment under Rule 24b-2 of the Exchange Act; [*] denotes omissions. |
added to such approved suppliers list. The Parties may from time to time agree on materials that can be sourced by the Supplier from different sub-suppliers without GEHCs consent.
5. | Additional Suppliers |
The Supplier shall, at GEHCs written request, provide reasonable assistance to GEHC with regard to GEHCs efforts to have a designated alternative supplier for the Products (i) by providing GEHC or such designee with copies of all written SOPs and access at Suppliers facility to completed batch records or other tangible forms of recorded manufacturing documentation of the Products, that are reasonably necessary for the manufacture of the Product, and (ii) by making relevant personnel available within reason for consultation on the phone or at Suppliers facility with respect to clauses (i) above.
6. | Forecast and Commitment |
a. | Forecasting. [*] ([*]) days before the end of each quarter, GEHC shall submit to the Supplier in writing a [*] ([*]) month rolling quarterly forecast (Forecast) for its estimated needs of the Products during the subsequent [*] ([*]) month period. Supplier shall use the Forecast as the basis for its production planning and shall adjust the Safety Stock according to the new Forecast within the agreed lead times. In the event that GEHC does not timely submit a Forecast to the Supplier, Supplier will notify GEHC in writing and GEHC will have [*] ([*]) business days to provide the Supplier with the updated Forecast or if GEHC fails to provide the updated Forecast, the Forecast will revert to [*] ([*]). |
b. | The Forecast. The [*] of every Forecast provided by GEHC for Products shall be [*] on GEHC and the Supplier. [*]. The Supplier agrees to use all commercially reasonable efforts to be responsive and supply Product in excess of any firm and binding [*] if so requested by GEHC, provided such excess shall not exceed [*]% of the then firm and binding [*]. |
c. | General Supply Commitment. The Supplier represents and warrants that it has the capacity and expertise necessary to [*]. In the event that the market demand exceeds this volume, GEHC and Supplier will work together and make best efforts to meet the market demand. |
d. | Purchase Commitment. As a result of this Agreement, the Supplier will become one of the preferred suppliers of GEHC for the Products. GEHC agrees that the [*] shall include quantities of the Products, which corresponds to at least [*] ([*]) percent of GEHCs total actual requirements in [*] for the Products. For any year thereafter the requirement in the [*] shall be at least [*] ([*]) percent of GEHCs total actual requirements in [*] for the Products per year and at least [*] ([*]) percent of GEHCs actual requirements in [*] of each of the Products. While GEHC has to adjust its production levels to market changes GEHC shall use all reasonable efforts to distribute orders evenly during the year and to avoid to have quarters without any orders at all. Further, GEHC agrees to purchase at least [*] ([*]) percent of its total requirements in [*] of the Products during the years [*] of this Agreement or any shortened period of [*] in the event this Agreement is terminated in accordance with 16.6 and 16.7 in Attachment E. In the event GEHC should fail to fulfill its purchase obligations hereunder it shall as its sole liability immediately issue a purchase order for the missing quantities upon the Suppliers written request thereto. The Supplier agrees to maintain the equivalent ability to manufacture the Products for GEHC. The Parties may from time to time mutually agree in writing on separate arrangements for certain time periods in order to accommodate specific requirement and planning needs which may deviate from the above commitment. GEHC shall be free to decide on the mix between Products under the above purchase obligations and in the [*] forecast, provided that the binding part of the forecast shall be fixed. In the event there is a requirement in excess of [*]% of the firm and committed [*] and the Supplier is unable to deliver within the agreed lead times as specified in Attachment C then GEHC shall be free to purchase any such additional quantities as Supplier is unable to deliver that [*] from other suppliers. |
Strategic Supplier Alliance Agreement - GEHC Directs EMEA Contract Manufacturing / Version Supply 1.0 | 16 (30) | |
Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Companys application requesting confidential treatment under Rule 24b-2 of the Exchange Act; [*] denotes omissions. |
If the Supplier during a certain [*] is unable to timely supply Products complying with agreed quality standards in quantities specified in GEHCs committed Forecast, then GEHCs purchasing commitment hereunder shall be reduced with a quantity corresponding to the quantity to which such inability relates.
e. | No Obligation. Other than as set out in subsection b) and d) above, it is the express understanding of the Parties that GEHC shall have no obligation to purchase Products exclusively from the Supplier or to purchase any minimum amount of Products, and may use other suppliers for any and all Products, or similar products. |
7. | Contract Managers and Communication |
a. | Contract Manager. Both the Supplier and GEHC will appoint a contract manager to manage their respective obligations under this Agreement, to act as focal points between the two organizations and review progress on a quarterly basis. The contract manager shall be as specified below or such other person as subsequently communicated to the other Party. |
GEHC: | [*] | |
Supplier: | [*] |
b. | Legal Notices (as set forth in Section 18 in Attachment E). |
GEHC: | Björkgatan 30 | |
751 84 Uppsala, Sweden | ||
Fax No. [*] | ||
Supplier: | 41 Seyon Street Bldg #1 suite 100 | |
Waltham, MA 02453 USA | ||
Phone: 781 ###-###-#### (main) | ||
Fax: 781 ###-###-#### |
c. | Crisis Communication. The Supplier must maintain the ability to contact or receive contact from GEHC on a twenty-four (24) hour per day, seven (7) days per week basis in order to communicate and manage crisis situations that threaten to or interrupt the supply chain. |
8. | Insurance and Liability |
a. | The Supplier undertakes to maintain a comprehensive liability insurance policy with a reputable insurer including cover for third party liability and product liability on terms customary to the business. Such insurance shall be for an insured sum of not less than USD [*] ([*])[*] and the Supplier shall supply GEHC with a copy of the relevant policy on request. |
b. | The Supplier shall be liable to compensate GEHC for direct and indirect damage and loss it has caused GEHC under this Agreement up to USD [*] ([*])[*]. In the event of any loss or damage in excess of this amount the Supplier shall not be liable to compensate for such excess damage or loss, unless: (i) caused by its gross negligence or willful misconduct, (ii) caused by its breach of confidentiality obligations under this Agreement, or (iii) relating to its intellectual property indemnification obligations under this Agreement. |
9. | Safety Stock and Consignment Stock |
The Supplier shall keep a Safety Stock at the Suppliers premises, corresponding to the minimum set inventory values and the replenishment times in Attachment C.
The inventory levels stated in Attachment C shall be based on the latest [*] Forecast distributed by GEHC. In case a new Forecast leads to replenishment actions for the safety stock the Supplier shall use
Strategic Supplier Alliance Agreement - GEHC Directs EMEA Contract Manufacturing / Version Supply 1.0 | 17 (30) | |
Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Companys application requesting confidential treatment under Rule 24b-2 of the Exchange Act; [*] denotes omissions. |
all commercially reasonable efforts to replenish the Safety Stock as soon as practical and always within the agreed lead times set forth in Attachment C.
GEHC is reviewing the possibility to introduce a consignment stock arrangement, ie having the Supplier to own certain stock of Product at GEHC premises. The Supplier agrees to negotiate the terms and conditions in good faith.
10. | Manufacturing Process |
For clarity it is stated that all written manufacturing or production documentation relating solely to the Products, including without limitation the manufacturing documents specified in Attachment F shall be the sole property of GEHC. The Supplier shall document and GEHC shall have access to review all written manufacturing or production records relating to any of the Products at Suppliers facility and upon request from GEHC, the Supplier is obliged to send GEHC copies of the requested manufacturing or production documents (including SOPs and records) and such a request shall not be unreasonably withheld by the Supplier.
The Supplier shall keep a master list of production documents showing the name, identity and version number for each of the production documents that is used in the production of the Products. The Supplier shall always keep and maintain the master list of production documentation and shall send upon GEHCs request an update of any of the documents included in the master list of production documentation.
11. | Business interruption |
The Supplier undertakes to keep GEHC informed about any circumstances that might reasonably impact on the Suppliers ability to supply the Products, timely and in accordance with applicable quality standards, including any plans to close or divest the business relating to all or any of the Products. If such circumstance should arise or may reasonably be possible to arise the Supplier shall immediately inform GEHC and propose a plan on how to mitigate the consequences thereof. The Parties shall then in good faith conduct negotiations concerning the actions to be taken and the costs to avoid or mitigate the risks.
12. | Reports |
GEHC will provide Supplier within [*] of the close of each [*] period a report of the total quantity of each of the Products purchased by GEHC from all suppliers during the period.
The Supplier will provide GEHC with finished goods inventory and Safety Stock levels of Products within [*] of the close of each [*] period.
13. | Audit |
Supplier shall have the right to have an independent third party reasonably acceptable to GEHC, such as one of the global auditing firms, to conduct an annual audit of GEHCs records to ensure compliance with GEHCs commitments according to Section 6 d in this Section of the Agreement.
14. | Supply of GEHC products for the manufacture of Products |
During the term of this agreement the Supplier shall have the right to purchase the following products from GEHC at following price conditions:
Name | Article No: | Price: | ||
[*] |
Strategic Supplier Alliance Agreement - GEHC Directs EMEA Contract Manufacturing / Version Supply 1.0 | 18 (30) | |
Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Companys application requesting confidential treatment under Rule 24b-2 of the Exchange Act; [*] denotes omissions. |
Delivery conditions: CIF
Lead time: [*]
Credit term: [*] days from date of invoice
Order handling: all order shall be submitted to the Contract Manager, together with a declaration of the intended use for the Products.
The sale of the goods to the Supplier shall be subject to GEHC Conditions of Sale.
The products ordered in accordance with this Clause 15 may only be used in the manufacture of the Products for delivery to GEHC. Any other use of the products ordered is strictly forbidden.
15. | ELISA Kits |
GEHC acknowledges that the Supplier manufactures and sells ELISA analytic kits for protein leakage testing. During the term of this Agreement Repligen shall have the right to use MabSelect SuRe ligands and the MabSelect SuRe trademark, but only in connection with the manufacture, sale and marketing of ELISA analytical kits for protein leakage testing. The Supplier agrees to use the GEHC trademarks in accordance with GEHCs written instructions from time to time.
16. | Cell banks |
The biological starting material used in the fermentation process originates from the cell banks kept and owned by GEHC. Such material may only be used in connection with the manufacture of the Products and shall be returned to GEHC, alternatively destroyed upon termination of this agreement for what ever reason. Supplier shall not disclose or provide such material to any third parties, unless GEHC has given its prior written consent thereto. The Supplier agrees not to sequence, extract or in any other way use the plasmid, the chromosome or any of the DNA codes present in the cell banks.
The supplier may order starting material according to the following conditions:
a) | Lead time: [*] days, unless otherwise agreed. |
b) | Orders: written orders in accordance with form provided by GEHC specifying product, campaign, numbers of vials and requested delivery date. The order will be sent to: |
GE Healthcare Bio-Sciences AB |
Att: [*] |
BL3-2 |
Björkgatan 30 |
751 84 UPPSALA |
Sweden |
tel: | [*] | |
fax: | [*] |
c) | GEHC will confirm order without delay and provide a notice two weeks before the estimated delivery date. |
d) | Supplier shall confirm receipt of the cell bank. |
e) | Transportation: GEHC will coordinate with Repligen to ensure appropriate delivery time and arrangements for the cell banks and will arrange and pay for transportation. |
Documentation: The cell banks will be accompanied by a Certificate of Analysis in accordance with the documents listed in Attachment F.
Strategic Supplier Alliance Agreement - GEHC Directs EMEA Contract Manufacturing / Version Supply 1.0 | 19 (30) | |
Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Companys application requesting confidential treatment under Rule 24b-2 of the Exchange Act; [*] denotes omissions. |
f) | Repligen shall provide GEHC at the beginning of every [*] a report of the total quantity of seed stock for each of the Products as well as the planned consumption of the seed stock for the following [*] months. GEHC shall use this information for their internal planning purposes. |
17. | Other products |
The Parties have agreed to enter into a separate agreement covering the Supplier´s supply of [*]. The Parties intend to enter into a separate agreement concerning supply of [*].
Strategic Supplier Alliance Agreement - GEHC Directs EMEA Contract Manufacturing / Version Supply 1.0 | 20 (30) | |
Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Companys application requesting confidential treatment under Rule 24b-2 of the Exchange Act; [*] denotes omissions. |
Attachment E General Terms and Conditions
ORDER AND SUPPLY
Strategic Supplier Alliance Agreement - GEHC Directs EMEA Contract Manufacturing / Version Supply 1.0 | 21 (30) | |
Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Companys application requesting confidential treatment under Rule 24b-2 of the Exchange Act; [*] denotes omissions. |
Strategic Supplier Alliance Agreement - GEHC Directs EMEA Contract Manufacturing / Version Supply 1.0 | 22 (30) | |
Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Companys application requesting confidential treatment under Rule 24b-2 of the Exchange Act; [*] denotes omissions. |
Strategic Supplier Alliance Agreement - GEHC Directs EMEA Contract Manufacturing / Version Supply 1.0 | 23 (30) | |
Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Companys application requesting confidential treatment under Rule 24b-2 of the Exchange Act; [*] denotes omissions. |
Strategic Supplier Alliance Agreement - GEHC Directs EMEA Contract Manufacturing / Version Supply 1.0 | 24 (30) | |
Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Companys application requesting confidential treatment under Rule 24b-2 of the Exchange Act; [*] denotes omissions. |
Strategic Supplier Alliance Agreement - GEHC Directs EMEA Contract Manufacturing / Version Supply 1.0 | 25 (30) | |
Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Companys application requesting confidential treatment under Rule 24b-2 of the Exchange Act; [*] denotes omissions. |
Strategic Supplier Alliance Agreement - GEHC Directs EMEA Contract Manufacturing / Version Supply 1.0 | 26 (30) | |
Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Companys application requesting confidential treatment under Rule 24b-2 of the Exchange Act; [*] denotes omissions. |
Strategic Supplier Alliance Agreement - GEHC Directs EMEA Contract Manufacturing / Version Supply 1.0 | 27 (30) | |
Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Companys application requesting confidential treatment under Rule 24b-2 of the Exchange Act; [*] denotes omissions. |
Strategic Supplier Alliance Agreement - GEHC Directs EMEA Contract Manufacturing / Version Supply 1.0 | 28 (30) | |
Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Companys application requesting confidential treatment under Rule 24b-2 of the Exchange Act; [*] denotes omissions. |
Strategic Supplier Alliance Agreement - GEHC Directs EMEA Contract Manufacturing / Version Supply 1.0 | 29 (30) | |
Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Companys application requesting confidential treatment under Rule 24b-2 of the Exchange Act; [*] denotes omissions. |
Attachment F
GE Technology
Production know-how covering [*] with regard to rPA and ZätA protein, in particular as described in the following documentation.
Documentation title | GEHC Doc No. (when applicable) | |
rPA [*] | ||
ZätA [*] |
For avoidance of doubt, the above is not an exhaustive list of GE Technology, but describes certain key elements of the manufacturing process and test methods relating to the Products.
Strategic Supplier Alliance Agreement - GEHC Directs EMEA Contract Manufacturing / Version Supply 1.0 | 30 (30) | |
Portions of this Exhibit were omitted and have been filed separately with the Secretary of the Commission pursuant to the Companys application requesting confidential treatment under Rule 24b-2 of the Exchange Act; [*] denotes omissions. |