Receipt and Storage of cGMP Controlled Raw Materials Regulations and Best Practices
Abstract:Receipt and Storage of cGMP Controlled Raw Materials Regulations and Best Practices
Manufactures of drugs who lack a defined raw material processing have received FDA 483s and lost several batches of products. Designing the Receipt, Handling and Processing, Specification, Inventory Tracking, and Qualification of cGMP Controlled Raw Materials is critical to Life sciences personnel to gain drug approvals.
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