Sub-Part E - Control of Materials

5.0 - Materials Overview

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There shall be written procedures describing in sufficient detail the receipt, identification, storage, handling, sampling, testing, and approval or rejection of components and drug product containers and closures; such written procedures shall be followed. Components and drug product containers and closures shall at all times be handled and stored in a manner to prevent contamination.

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Components of a pharmaceutical waiting to be used by production, a red drum containing liquid, some brown powder, and boxes of packaging