Documentation of quality data Sample Clauses

Documentation of quality data. The SUPPLIER must document the quality data in accordance with the relevant requirements of ZEISS (quality records). This will include in particular: Documentation of the manufacturing data (inspection and testing reports, initial sample testing and inspection reports, quality control charts, process data from parameter monitoring, etc.); Documentation of the product lifecycle and reliability tests Documentation of test equipment monitoring. Feasibility study Corrective and preventive action ZEISS is entitled to have sight of the documentary evidence and obtain copies thereof. This also applies to sub-contractors' documents. All relevant documentary evidence must be archived for at least 10 years from the date of delivery of the GOODS and SERVICES and must be protected so that legibility is guaranteed during the retention period. Any further legal obligations regarding documentation and archiving remain unaffected hereby. Acceptance of goods / incoming inspection at ZEISS On the arrival of the GOODS and SERVICES, ZEISS will only check whether they correspond to the quantity and type ordered, whether there is visible external transport damage on the packaging or whether there are visible external defects. ZEISS will also normally undertake random checks of the quality documents / certificates which accompany the delivery. ZEISS reserves the right to conduct additional checks and tests on a case by case basis. The SUPPLIER must orient its Quality Management system and Quality Assurance measures to this reduced testing and inspection of incoming goods. ZEISS will inform the SUPPLIER in writing about defects on the GOODS and SERVICES which were delivered as soon as they are identified during the regular course of business. In this respect, the SUPPLIER will waive the objection of delay in lodging a complaint. Special release prior to the delivery of the GOODS and SERVICES to ZEISS If the SUPPLIER is unable to supply the GOODS and SERVICES as agreed in accordance with the contract by reason of non-conformities identified prior to delivery and if the deviations cannot be rectified by special efforts and emergency measures before the agreed delivery date, in truly exceptional cases the SUPPLIER may request approval for the delivery of non-conforming GOODS and SERVICES by means of an application for special release. Nevertheless, the urgency of the supply situation must always be first clarified with the person at ZEISS who placed the order and efforts made to rec...
Sample 1
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Documentation of quality data. ‌ The SUPPLIER must document the quality data in accordance with the relevant requirements of ZEISS (quality records). This will include in particular: - Documentation of the manufacturing data (inspection and testing reports, initial sample testing and inspection reports, quality control charts, process data from parameter monitoring, etc.); - Documentation of the product lifecycle and reliability tests - Documentation of test equipment monitoring. - Feasibility study - Corrective and preventive action ZEISS is entitled to have sight of the documentary evidence and obtain copies thereof. This also applies to sub-contractors' documents. All relevant documentary evidence must be archived for at least 10 years from the date of delivery of the GOODS and SERVICES and must be protected so that legibility is guaranteed during the retention period. Any further legal obligations regarding documentation and archiving remain unaffected hereby.
Sample 1

Related to Documentation of quality data

  • Documentation and compliance (a) The data importer shall promptly and adequately deal with enquiries from the data exporter that relate to the processing under these Clauses.

  • Documentation and Record Keeping 1. Records to be Maintained Subrecipient shall maintain all records required by the Federal regulations specified in 24 CFR 570.506 that are pertinent to the activities to be funded under this Contract. Such records shall include, but not be limited to:

  • Electronic and Information Resources Accessibility and Security Standards a. Applicability: The following Electronic and Information Resources (“EIR”) requirements apply to the Contract because the Grantee performs services that include EIR that the System Agency's employees are required or permitted to access or members of the public are required or permitted to access. This Section does not apply to incidental uses of EIR in the performance of the Agreement, unless the Parties agree that the EIR will become property of the State of Texas or will be used by HHSC’s clients or recipients after completion of the Agreement. Nothing in this section is intended to prescribe the use of particular designs or technologies or to prevent the use of alternative technologies, provided they result in substantially equivalent or greater access to and use of a Product.

  • Licensed Documentation If commercially available, Licensee shall have the option to require the Contractor to deliver, at Contractor’s expense: (i) one (1) hard copy and one (1) master electronic copy of the Documentation in a mutually agreeable format; (ii) based on hard copy instructions for access by downloading from the Internet

  • Dissemination of Research Findings and Acknowledgement of Controlled-Access Datasets Subject to the NIH GDS Policy It is NIH’s intent to promote the dissemination of research findings from use of controlled-access dataset(s) subject to the NIH GDS Policy as widely as possible through scientific publication or other appropriate public dissemination mechanisms. Approved Users are strongly encouraged to publish their results in peer-reviewed journals and to present research findings at scientific meetings.

  • Accessibility of Web-Based Information and Applications For State Agency Authorized User Acquisitions: Any web-based information and applications development, or programming delivered pursuant to the contract or procurement, will comply with New York State Enterprise IT Policy NYS-P08-005, Accessibility of Web-Based Information and Applications as follows: Any web-based information and applications development, or programming delivered pursuant to the contract or procurement, will comply with New York State Enterprise IT Policy NYS-P08- 005, Accessibility of Web-Based Information and Applications as such policy may be amended, modified or superseded, which requires that state agency web-based information and applications are accessible to persons with disabilities. Web-based information and applications must conform to New York State Enterprise IT Policy NYS-P08-005 as determined by quality assurance testing. Such quality assurance testing will be conducted by the State Agency Authorized User and the results of such testing must be satisfactory to the Authorized User before web-based information and applications will be considered a qualified deliverable under the contract or procurement.

  • Abbreviated Documentation Requirements Compile and submit:

  • Technical Documentation Prior to commencement of the Tests on Completion, the Contractor shall supply to the Engineer the technical documentation as specified in the Employer’s Requirements. The Works or Section shall not be considered to be completed for the purposes of taking- over under sub-clause 10.1 [Taking Over of the Works and Sections] until the Engineer has received the technical documentation as defined in this sub-clause 5.7, the "history file" including design calculations and certain certification as well as any other documents required to meet the CE Marking requirements.

  • Product Documentation You should review the policy documents carefully to ensure they accurately reflect the cover, conditions, limits, and other terms that you require. Particular attention should be paid to policy conditions and warranties as failure to comply with these could invalidate your policy. It is important that you retain and keep safely all documents associated with your policy so that you can refer to them in the event of a claim.

  • Marketing Materials (a) During the term of this Agreement, the Sub-Adviser agrees to furnish the Manager at its principal office for prior review and approval by the Manager all written and/or printed materials, including but not limited to, PowerPointÒ or slide presentations, news releases, advertisements, brochures, fact sheets and other promotional, informational or marketing materials (the “Marketing Materials”) for internal use or public dissemination, that are produced or are for use or reference by the Sub-Adviser, its affiliates or other designees, broker-dealers or the public in connection with the Series, and Sub-Adviser shall not use any such materials if the Manager reasonably objects in writing within five business days (or such other period as may be mutually agreed) after receipt thereof. Marketing Materials may be furnished to the Manager by first class or overnight mail, facsimile transmission equipment, electronic delivery or hand delivery.

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