21 CFR Part 99 - PART 99—DISSEMINATION OF INFORMATION ON UNAPPROVED/NEW USES FOR MARKETED DRUGS, BIOLOGICS, AND DEVICES
- 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)