21 CFR Chapter I, Subchapter D - DRUGS FOR HUMAN USE

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There are 332 Updates appearing in the Federal Register for Title 21. View below or at eCFR (GPOAccess)

Title 21 published on 2015-12-03

The following are ALL rules, proposed rules, and notices (chronologically) published in the Federal Register relating to Title 21 after this date.

* Only displaying the most recent 50 entries for Title 21. Please, view a Part for the full list of changes within that Part.

  • 2017-01-19; vol. 82 # 12 - Thursday, January 19, 2017
    1. 82 FR 6367 - Manufacturer Communications Regarding Unapproved Uses of Approved or Cleared Medical Products; Availability of Memorandum; Reopening of the Comment Period
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      DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration
      Reopening of comment period related to public hearing; availability of memorandum.
      Submit either electronic or written comments by April 19, 2017.
      21 CFR Part 15

Title 21 published on 2015-12-03.

The following are only the Rules published in the Federal Register after the published date of Title 21.

For a complete list of all Rules, Proposed Rules, and Notices view the Rulemaking tab.

* Only displaying the most recent 50 entries for Title 21. Please, view a Part for the full list of changes within that Part.

  • 2017-01-13; vol. 82 # 9 - Friday, January 13, 2017
    1. 82 FR 4151 - Cardiovascular Devices
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      DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration
      21 CFR Part 870