Traceability and documentation. On the delivery note for each Product, Gables will provide a certificate of conformance to all appropriate specifications and design data. For parts manufactured under FAA PMA or FAA Technical Standard Order, Gables may provide an 8130-3 tag upon request.
Traceability and documentation. The supplier is obligated to provide the necessary QA documentation which enables traceability of parts with special features. In the case of a detected error, traceability must be so sufficiently docu‐ mented that it is possible to limit the amount of defective parts produced. For the creation and storage of documents the recommendations from VDA (Volume 1 "Verification") in the currently valid version are to be implemented. Documents requiring special archiving, in particu‐ lar those concerning security‐relevant features, must be archived for 15 years, other documents for at least 3 years. In the case of claims by third parties, the supplier shall provide CarboFibretec with access to the rele‐ vant quality assurance documentation necessary to defend itself against said claims. The documents shall be surrendered temporarily, however for as long as they are needed in order to furnish exonerat‐ ing evidence.
Traceability and documentation. The supplier undertakes to provide proof of QS documentation required for traceability of parts with significant characteristics. In case of a detected deviation, traceability must be possible in such a way as to limit the quantity of defective parts. Elektra will provide the supplier with the data required for traceability. For the creation and storage of documents, the recommendation of the VDA (Volume 1 "Verification") in the currently valid version must be taken into consideration Documents (D-Parts) with special ar- chiving that relate to special security-relevant features must be archived for 15 years, other documents at least 3 years. In the event of claims by third parties, the Supplier shall grant Elektra access to the relevant quality documentation for the defense against claims and shall make them temporarily available as far as necessary for the execution of the documentation.
Traceability and documentation. Traceability is key to assuring the appropriate provenance of cells and tissues used for biological assays. This is achieved by the implementation of a documentation system to track the cells and tissues from procurement to use in an assay. Accurate records for all stages of this process will often be documented in forms, standard operating procedures etc., and these can also be used to facilitate the analysis and replication of laboratory work. Templates for documenting the tissues used in experimental work can be found in Coecke et al. (2005). The stages of the process should be mapped out to include procurement, receipt of biological material, processing the material, performing assays using the material and finally, disposal of the materials. Documentation should be put in place to cover the complete process.
Traceability and documentation. The supplier undertakes to provide evidence a of QS documentation system, which is required to ensure the traceability of parts with specific characteristics. Should a defect be found, traceability must be possible to the extent that a limitation of the number of damaged parts is feasible. The customer and the supplier will come to an agreement on the amount of data needed to achieve this goal and the required level of traceability. For guidance on the creation and storage of documents, see the latest version of the VDA recommendations (Vol. 1 “Documentation and archiving”). Documents with specific archiving requirements, particularly those with safety-related characteristics (CC's) must be archived for a period of 15 years, other documents for at least 3 years. In cases where the customer may be required to fend off claims by third parties, the supplier must grant him access to the relevant quality documentation and also hand over this documentation for a limited period should it be required by the customer as exonerating evidence.
Traceability and documentation. The supplier agrees to maintain QS documentation required for tracing parts with specific characteristics. If defects are found, QS documentation must allow parts to be traced to a specific quantity of parts that, if defective, may then be contained. The supplier and Seuffer will agree on the required data and the degree of traceability. The VDA recommendations (vol. 1 "Nachweisführung / Verification Management") in the respectively valid version shall be taken into consideration for preparing and archiving documents. Documents with particular archiving requirements, e.g. for critical characteristics (CCs), must be retained for 15 years, other must be archived for at least three years. In the event third parties take legal action against Seuffer, the supplier will xxxxx Xxxxxxx access to any required pertinent quality documentation available to support Seuffer's defense and, where required for such defense action, will make the documentation available temporarily to Seuffer.
Traceability and documentation
