Federal (United States) · Regulations
Subpart C
13 sections
13 sections
- 21 C.F.R. § 251.9Registration of Foreign Sellers.
- 21 C.F.R. § 251.10Reviewing and updating registration information for Foreign Sellers.
- 21 C.F.R. § 251.11Official contact and U.S. agent for Foreign Sellers.
- 21 C.F.R. § 251.12Importer responsibilities.
- 21 C.F.R. § 251.13Labeling of eligible prescription drugs.
- 21 C.F.R. § 251.14Supply chain security requirements for eligible prescription drugs.
- 21 C.F.R. § 251.15Qualifying laboratory requirements.
- 21 C.F.R. § 251.16Laboratory testing requirements.
- 21 C.F.R. § 251.17Importation requirements.
- 21 C.F.R. § 251.18Post-importation requirements.
- 21 C.F.R. § 251.19Reports to FDA.
- 21 C.F.R. § 251.20Severability.
- 21 C.F.R. § 251.21Consequences for violations.