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2.1 - Production & Quality Management

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There shall be a quality control unit that shall have the responsibility and authority to approve or reject all components, drug product containers, closures, in-process materials, packaging material, labeling, and drug products, and the authority to review production records to assure that no errors have occurred or, if errors have occurred, that they have been fully investigated

GMP-SOP-Download Drug2.0 - Personnel Overview
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GMP-SOP-Download Drug2.2 - Personnel Training
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Regular price Sale price £19.99 GBP