StacksVerified U.S. regulatory reference

21 CFR §601.30

Verified against eCFR.gov as of June 20, 2026View official text on eCFR.gov
This subpart applies to radiopharmaceuticals intended for in vivo administration for diagnostic and monitoring use. It does not apply to radiopharmaceuticals intended for therapeutic purposes. In situations where a particular radiopharmaceutical is proposed for both diagnostic and therapeutic uses, the radiopharmaceutical must be evaluated taking into account each intended use.