21 C.F.R. § 203.32

Drug sample storage and handling requirements.

Last amended: 2016Year: 2026Length: 86 wordsSubsections: 1Official source

Cite as 21 C.F.R. § 203.32 (2026)

(a) Storage and handling conditions. Manufacturers, authorized distributors of record, and their representatives shall store and handle all drug samples under conditions that will maintain their stability, integrity, and effectiveness and ensure that the drug samples are free of contamination, deterioration, and adulteration. (b) Compliance with compendial and labeling requirements. Manufacturers, authorized distributors of record, and their representatives can generally comply with this section by following the compendial and labeling requirements for storage and handling of a particular prescription drug in handling samples of that drug.
21 C.F.R. § 203.32: Drug sample storage and handling requirements. | Justis AI