The 21 CFR 211 Drug cGMP Quality Program Manual: SOP Architecture, Batch Record Systems, Deviation and CAPA Workflows, and Inspection-Readiness Tools for Pharmaceutical Manufacturing Quality Teams

Name: The 21 CFR 211 Drug cGMP Quality Program Manual: SOP Architecture, Batch Record Systems, Deviation and CAPA Workflows, and Inspection-Readiness Tools for Pharmaceutical Manufacturing Quality Teams
Brand: Independently published

Independently published

Pages: 291, Paperback, Independently published

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