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  2. Title 21 of the Code of Federal Regulations - Wikipedia

    en.wikipedia.org/wiki/Title_21_of_the_Code_of...

    Title 21 is the portion of the Code of Federal Regulations that governs food and drugs within the United States for the Food and Drug Administration (FDA), the Drug Enforcement Administration (DEA), and the Office of National Drug Control Policy (ONDCP). [1] It is divided into three chapters: Chapter I — Food and Drug Administration

  3. Device Master Record - Wikipedia

    en.wikipedia.org/wiki/Device_Master_Record

    The following contents are listed in the relevant chapter of the CFR [1] as part of ... Code of Federal Regulations Title 21, Sec. 820.181 Device master record ...

  4. 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 ...

  5. Code of Federal Regulations - Wikipedia

    en.wikipedia.org/wiki/Code_of_Federal_Regulations

    "About Code of Federal Regulations". Government Publishing Office. 9 March 2017. "A Research Guide to the Federal Register and the Code of Federal Regulations". Law Librarians' Society of Washington, D.C. July 21, 2012. "Report to Congress on the Costs and Benefits of Federal Regulations". Office of Management and Budget. September 30, 1997.

  6. Quality management system - Wikipedia

    en.wikipedia.org/wiki/Quality_management_system

    The rule is promulgated at 21 CFR 820. [ 5 ] According to current Good Manufacturing Practice (GMP), medical device manufacturers have the responsibility to use good judgment when developing their quality system and apply those sections of the FDA Quality System (QS) Regulation that are applicable to their specific products and operations, in ...

  7. Design controls - Wikipedia

    en.wikipedia.org/wiki/Design_controls

    Download as PDF; Printable version; ... (21 CFR 820.30). At a high level, this regulation requires: ... Text is available under the Creative Commons Attribution ...

  8. Electronic lab notebook - Wikipedia

    en.wikipedia.org/wiki/Electronic_lab_notebook

    Typical provisions related to software validation are included in the medical device regulations at 21 CFR 820 (et seq.) [8] and Title 21 CFR Part 11. [9] Essentially, the requirements are that the software has been designed and implemented to be suitable for its intended purposes.

  9. File:97-820 (IA 97-820-crs).pdf - Wikipedia

    en.wikipedia.org/.../File:97-820_(IA_97-820-crs).pdf

    Image title Russian government decisions and the budget deficit crisis have hit the Ministry of Defense very hard, cutting defense spending drastically and transforming the Defense Ministry into a residual claimant on scarce resources.