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The 21 CFR 211 Drug cGMP Quality Program Manual
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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
Buch (broschiert)ca. 211.00 CHF
lieferbar in ca. 15 Arbeitstagen
Juli 2026, ca. 292 Seiten, Englisch
Independently Published
979-8-1856-3587-2

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