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. They must at all times be handled and stored in a manner to prevent contamination
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Vendor:GMP-SOP-Download Drug
5.0 - Materials Overview
Regular price $26.00 USDRegular price -
Vendor:GMP-SOP-Download Drug
5.1 - Supplier Approval and Control
Regular price $26.00 USDRegular price -
Vendor:GMP-SOP-Download Drug
5.2 - Materials - Receipt and Storage
Regular price $26.00 USDRegular price -
Vendor:GMP-SOP-Download Drug
5.3 - Materials - Sampling and Testing
Regular price $26.00 USDRegular price

