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. Activities The design validation activity will be shared across all partner companies however. Specific validation tasks are shown in the RASIC. [***] B-12 Telematics Specification Strictly Confidential Telematics Specification Document - 2.6 Purchasing Activities Purchase requests will be made via SEV US for Project NRE and parts for DOE platforms. SEV UK will place purchase requests for LCVPP since they are currently separate financial entities. 3 COST 3.1 Fixed and Operating Costs More to be added – pending confirmation of spec for [***]. Table 3 - Fixed and Operating cost Summary 3.2 Bulk Purchase and Economies of Scale The supplier will provide volume pricing summary to Xxxxx Electric Vehicles. B-13 Telematics Specification Strictly Confidential Telematics Specification Document - 4 Product Description 4.1 Hero Card 4.2 Concept The system comprises a Remote Device, GPRS network, Server, Web Interface and Storage Unit. The Remote Device (RD) will observe directly defined set of [***], [***]and [***]based signals which will vary dependent upon [***] signal source generator as a function of supplier choice. These signals will then be transmitted via Global Packet Radio Service (GPRS) for handling and display by the server using a Web Interface. The RD shall also determine the operational state of other consumable domestic systems such as HVAC. Figure 1 - System Architecture - Xxxxxx 120kW, ENOVA based system as example Telemetry Delivers o Improved customer focus, shareholder value, customer service and satisfaction o Increased understanding of vehicle/system performance indicators/parameters o Increased understanding of customer usage profiles o Increased efficiencies in SEV logistics o Warranty Cost Reduction o The foundation for a Saleable Remote Asset Management System o Potential to be used as an EOL Process o Compliance with USA and UK funding body data mining requirements [***]
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. 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. Scivanta is responsible for determining the product functions required for clinical efficacy. Ethox will assist Scivanta to translate and document these product requirements into system and device specifications for Ethox’s prototyping and manufacturing. Ethox is responsible for engineering, testing and manufacturing of prototypes and products to assure functional specifications are met. Ethox is further responsible for the completion of all tasks necessary to obtain FDA and EMEA approval, as well as any other regulatory approval needed for the HCMS. Scivanta is responsible for clinical testing of prototypes and products to assure market requirements are met.
Design Validation. Activities The design validation activity will be shared across all partner companies however. Specific validation tasks are shown in the RASIC. [***]
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 -------------------------------------------------------------------------------- 10 OF 16 -------------------------------------------------------------------------------- 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)
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. (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
