21 CFR § 211.105 Current Good Manufacturing Practice for Finished Pharmaceuticals

§ 211.105 Equipment identification.

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

(a) All compounding and storage containers, processing lines, and major equipment used during the production of a batch of a drug product shall be properly identified at all times to indicate their contents and, when necessary, the phase of processing of the batch.

(b) Major equipment shall be identified by a distinctive identification number or code that shall be recorded in the batch production record to show the specific equipment used in the manufacture of each batch of a drug product. In cases where only one of a particular type of equipment exists in a manufacturing facility, the name of the equipment may be used in lieu of a distinctive identification number or code.

← § 211.103 Calculation of yield.§ 211.110 Sampling and testing of in-process materials and drug products. →