21 Cfr Part 820 Pdf

by

View Title 21 on govinfo.gov; View Title 21 Section 820.30 PDF; These links go to the official, published CFR, which is updated annually. As a result, it may not include the most recent changes applied to the CFR. You can learn more about the process here.

  1. 21 Cfr 820 Part 11 Pdf
  2. 21 Cfr Part 820 Pdf
21 cfr 820 part 11 pdf
  1. 21 CFR § 820 US FDA QUALITY SYSTEM REGULATION ISO SPECIFIC DIFFERENCES 820.1 Scope 1 Scope 820.5 Quality System Each manufacturer shall establish and maintain a quality system that is appropriate for the specific medical device(s) designed or manufactured, and that meets the requirements of this part. 4.1.1 Quality management.
  2. 21 CFR 820 Basic Introduction. Errors that could be encountered as part of their job. Design and Development Subsystem. 820.30 Design Controls. 820.70(b) Production.
  3. 21 CFR 820 Basic Introduction. Errors that could be encountered as part of their job. Design and Development Subsystem. 820.30 Design Controls. 820.70(b) Production.
  • Table of Contents

    The in-page Table of Contents is available only when multiple sections are being viewed.

    Use the navigation links in the gray bar above to view the table of contents that this content belongs to.

  • Timeline

    No changes found for this content after 1/03/2017.

  • Go to Date
  • Compare Dates
  • Subscribe

    Subscribe to: Changes in Title 21 :: Chapter I :: Subchapter H :: Part 820 :: Subpart C :: Section 820.30

    Enhanced Content - Subscribe
  • Share
  • Published Edition

    View the most recent official publication:

    These links go to the official, published CFR, which is updated annually. As a result, it may not include the most recent changes applied to the CFR. You can learn more about the process here.

  • Display Options

    By default, the eCFR is displayed with paragraphs split and indented to follow the hierarchy of the document (“Enhanced Display”). This is an automated process for user convenience only and is not intended to alter agency intent or existing codification.

    The eCFR also offers a “Drafting Display”, where the paragraphs shown match the original CFR text. If you work for a Federal Agency, you should use the “Drafting Mode” when authoring amendatory language for inclusion in the Federal Register when developing amendatory instructions.

  • Print
  • Developer Tools

    This document is available in the following developer friendly formats:

    Information and documentation can be found in our developer resources.

21 cfr part 820
21 U.S.C. 351, 352, 360, 360c, 360d, 360e, 360h, 360i, 360j, 360l, 371, 374, 381, 383; 42 U.S.C. 216, 262, 263a, 264.
Part

21 Cfr 820 Part 11 Pdf

61 FR 52654, Oct. 7, 1996, unless otherwise noted.

21 Cfr Part 820 Pdf

{'United States Code': [{'Title': '21', 'Section': '351', 'headtext': ' Adulterated drugs and devices', 'cleanpath': '/uscode/text/21/351'}, {'Title': '21', 'Section': '352', 'headtext': ' Misbranded drugs and devices', 'cleanpath': '/uscode/text/21/352'}, {'Title': '21', 'Section': '360', 'headtext': ' Registration of producers of drugs or devices', 'cleanpath': '/uscode/text/21/360'}, {'Title': '21', 'Section': '360c', 'headtext': ' Classification of devices intended for human use', 'cleanpath': '/uscode/text/21/360c'}, {'Title': '21', 'Section': '360d', 'headtext': ' Performance standards', 'cleanpath': '/uscode/text/21/360d'}, {'Title': '21', 'Section': '360e', 'headtext': ' Premarket approval', 'cleanpath': '/uscode/text/21/360e'}, {'Title': '21', 'Section': '360h', 'headtext': ' Notification and other remedies', 'cleanpath': '/uscode/text/21/360h'}, {'Title': '21', 'Section': '360i', 'headtext': ' Records and reports on devices', 'cleanpath': '/uscode/text/21/360i'}, {'Title': '21', 'Section': '360j', 'headtext': ' General provisions respecting control of devices intended for human use', 'cleanpath': '/uscode/text/21/360j'}, {'Title': '21', 'Section': '360l', 'headtext': ' Postmarket surveillance', 'cleanpath': '/uscode/text/21/360l'}, {'Title': '21', 'Section': '371', 'headtext': ' Regulations and hearings', 'cleanpath': '/uscode/text/21/371'}, {'Title': '21', 'Section': '374', 'headtext': ' Inspection', 'cleanpath': '/uscode/text/21/374'}, {'Title': '21', 'Section': '381', 'headtext': ' Imports and exports', 'cleanpath': '/uscode/text/21/381'}, {'Title': '21', 'Section': '383', 'headtext': ' Office of International Relations', 'cleanpath': '/uscode/text/21/383'}], 'Statutes at Large': [], 'Public Laws': [], 'Presidential Documents': []}