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
Von:
Prescott, JamesJuli 2026, ca. 292 Seiten, Englisch
Independently Published
979-8-1856-3587-2
Independently Published
979-8-1856-3587-2
Juli 2026, ca. 292 Seiten, Englisch
Independently Published
979-8-1856-3587-2
Independently Published
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