Design Validation. Developer shall perform design validation to ensure that the East End Crossing conforms to defined user needs and requirements. The Design QA/QC Plan shall identify appropriate validation procedures.
Design Validation. Mxxxx shall establish and maintain procedures for Validating the design of the Product(s). Design Validation shall be performed under defined operating conditions on initial production units, Lots or batches, or their equivalents. Design Validation shall ensure that the Product(s) conforms to defined user needs and intended uses, and shall include testing of the Product(s) under actual or simulated use conditions. Results of Design Validation shall be documented in the DHF.
Design Validation. The Structure design and drawing should be duly verified by a licensed Structural designer before installation for all types of structure arrangements including the extension made, as per specification.
Design Validation. Design validation shall be performed upon completion of construction of every major component of the Infrastructure to determine if the final product is capable of meeting the objectives and requirements for the specified application or intended use. Project Co shall retain a permanent record of all validation reviews.
Design Validation. The purpose of this stage is to review and approve the Supplier’s deliverables to ensure that product and process quality are reached and in line with GFMS requirements. During this stage a formal Design Review has to be organized leading to a technical agreement. Proof of concept samples parts may be asked to confirm feasibility. Deliverables To be provided by To be approved by Design Review (Drawing, Technical data sheet…) GFMS R&D/Supplier GFMS R&D/Supplier Identification and approval of Critical Characteristics GFMS R&D/Supplier GFMS R&D, QUA/Supplier Proof of concept samples/prototypes Supplier GFMS R&D, QUA Draft Control Plan Supplier GFMS R&D, QUA
Design Validation. (DV) PLAN The DV plan will be written in Phase 2 of the project and will be delivered as part of the E2 deliverables. This plan will be based on a test matrix describing the test to be performed, what number of units are to be measured, and the parameters to be tested. REVISION: 02 PART NUMBER: 120337-01 CERTAIN CONFIDENTIAL INFORMATION CONTAINED IN THIS DOCUMENT, MARKED BY BRACKETS, HAS BEEN OMITTED AND FILED SEPARATELY WITH THE SECURITIES AND EXCHANGE COMMISSION PURSUANT TO RULE 24b-2 OF THE SECURITIES EXCHANGE ACT OF 1934, AS AMENDED. [ENDWAVE LOGO] powering broadband access
Design Validation. When the product being designed by the Supplier is the finished medical device and/or a stand-alone accessory to a finished medical device capable of operating independently, the Supplier shall have written procedures for validating the product design. Design validation shall be performed under defined operating conditions on initial production units, lots, or batches, or their equivalents. Design validation shall ensure that product conforms to defined user needs and intended uses and shall include testing of production units under actual or simulated use conditions. Design validation shall include software validation and risk analysis, where appropriate. The results of the design validation, including identification of the design, method(s), the date, and the individual(s) performing the validation, shall be documented. G.
Design Validation. This demonstrates that functional requirements align with the SHAMAN Reference Architecture and vice versa.
Design Validation. Traceability analysis: 1 person effort to produce a statement that the Reference Architecture incorporates the functional requirements for the demonstrators, as these derive from the use
Design Validation. Activities The design validation activity will be shared across all partner companies however. Specific validation tasks are shown in the RASIC. [***]
