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  2. System Design Review - Wikipedia

    en.wikipedia.org/wiki/System_Design_Review

    The SDR is a technical review conducted to evaluate the manner in which a project's system requirements have been allocated to configuration items, manufacturing considerations, next phase planning, production plans, and the engineering process that produced the allocation. This review is conducted when the system definition is at a point where ...

  3. Rohm and Haas Corporate Headquarters - Wikipedia

    en.wikipedia.org/wiki/Rohm_and_Haas_Corporate...

    The Rohm and Haas Corporate Headquarters was conceived as part of the city of Philadelphia's plan to improve and revive the area around Independence Hall.Along with the creation of a park north of Independence Hall, the area saw the construction of new and modern buildings including a federal courthouse, a new Philadelphia Mint and the Rohm and Haas Building. [5]

  4. Design review (U.S. government) - Wikipedia

    en.wikipedia.org/wiki/Design_review_(U.S...

    Design review is also required of medical device developers as part of a system of design controls described in the US Food and Drug Administration's governing regulations in 21CFR820. In 21CFR820.3(h), design review is described as "documented, comprehensive, systematic examination of the design to evaluate the adequacy of the design ...

  5. Design review - Wikipedia

    en.wikipedia.org/wiki/Design_Review

    The ultimate design review, if successful, therefore triggers the product launch or product release. The conduct of design reviews is compulsory as part of design controls, when developing products in certain regulated contexts such as medical devices. By definition, a review must include persons who are external to the design team.

  6. Independent reviewer - Wikipedia

    en.wikipedia.org/wiki/Independent_reviewer

    The US Food and Drug Administration requires that developers of medical device follow a system of design controls.A key part of this system is design review, defined in 21CFR820.3 section (h) as "a documented, comprehensive, systematic examination of the design to evaluate the adequacy of the design requirements, to evaluate the capability of the design to meet these requirements, and to ...

  7. Software inspection - Wikipedia

    en.wikipedia.org/wiki/Software_inspection

    The goal of the inspection is to identify defects. Commonly inspected work products include software requirements specifications and test plans. In an inspection, a work product is selected for review and a team is gathered for an inspection meeting to review the work product. A moderator is chosen to moderate the meeting.

  8. Richards Medical Research Laboratories - Wikipedia

    en.wikipedia.org/wiki/Richards_Medical_Research...

    The Goddard Laboratories, which are connected to the Richards Laboratories, have a similar appearance. When the University of Pennsylvania decided it needed a new medical research building, the dean of fine arts recommended Louis Kahn, a highly regarded professor of architecture on the faculty there who had been exploring new approaches for modern architecture.

  9. Verification and validation - Wikipedia

    en.wikipedia.org/wiki/Verification_and_validation

    Verification is intended to check that a product, service, or system meets a set of design specifications. [6] [7] In the development phase, verification procedures involve performing special tests to model or simulate a portion, or the entirety, of a product, service, or system, then performing a review or analysis of the modeling results. In ...