21 CFR 99 - DISSEMINATION OF INFORMATION ON UNAPPROVED/NEW USES FOR MARKETED DRUGS, BIOLOGICS, AND DEVICES
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- SUBPART A — General Information (§§ 99.1 - 99.3)
- SUBPART B — Information To Be Disseminated (§§ 99.101 - 99.105)
- SUBPART C — Manufacturer's Submissions, Requests, and Applications (§§ 99.201 - 99.205)
- SUBPART D — FDA Action on Submissions, Requests, and Applications (§§ 99.301 - 99.305)
- SUBPART E — Corrective Actions and Cessation of Dissemination (§§ 99.401 - 99.405)
- SUBPART F — Recordkeeping and Reports (§§ 99.501 - 99.501)
Source: 63 FR 64581, Nov. 20, 1998, unless otherwise noted.
Title 21 published on 2011-04-01
no entries appear in the Federal Register after this date.
This is a list of United States Code sections, Statutes at Large, Public Laws, and Presidential Documents, which provide rulemaking authority for this CFR Part.
This list is taken from the Parallel Table of Authorities and Rules provided by GPO [Government Printing Office].
It is not guaranteed to be accurate or up-to-date, though we do refresh the database weekly. More limitations on accuracy are described at the GPO site.
