21 CFR § 211.113 Current Good Manufacturing Practice for Finished Pharmaceuticals

§ 211.113 Control of microbiological contamination.

Current through Sep 8, 2026 · Read all of Part 211

(a) Appropriate written procedures, designed to prevent objectionable microorganisms in drug products not required to be sterile, shall be established and followed.

(b) Appropriate written procedures, designed to prevent microbiological contamination of drug products purporting to be sterile, shall be established and followed. Such procedures shall include validation of all aseptic and sterilization processes.

[43 FR 45077, Sept. 29, 1978, as amended at 73 FR 51932, Sept. 8, 2008]

← § 211.111 Time limitations on production.§ 211.115 Reprocessing. →