PART 99—DISSEMINATION OF INFORMATION ON UNAPPROVED/NEW USES FOR MARKETED DRUGS, BIOLOGICS, AND DEVICES
- SUBPART A—General Information (§99.1 to §99.3)
- SUBPART B—Information To Be Disseminated (§99.101 to §99.105)
- SUBPART C—Manufacturer's Submissions, Requests, and Applications (§99.201 to §99.205)
- SUBPART D—FDA Action on Submissions, Requests, and Applications (§99.301 to §99.305)
- SUBPART E—Corrective Actions and Cessation of Dissemination (§99.401 to §99.405)
- SUBPART F—Recordkeeping and Reports (§99.501 to §99.501)