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  5. 5.0 - Materials Overview
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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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GMP-SOP-Download Drug4.0 - Equipment Overview
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GMP-SOP-Download Drug5.1 - Supplier Approval and Control
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$26.00 USD