21 CFR Part 211 - Current Good Manufacturing Practice
Subpart E - Control of Components and Drug Product Containers/Closures

21 CFR Part 211 - Current Good Manufacturing Practice CFR211-E-80: Section 211.80 - General Requirements

Written procedures describing receipt, identification, storage, handling, sampling, testing, and approval or rejection of components and drug product containers and closures.

Maintained by Gerard BlokdykVerified against the published standard Control text last updated

Other controls in Subpart E - Control of Components and Drug Product Containers/Closures

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