21 CFR 11, 210/211, 606, 820 - Electronic Records with Drug, Blood and Device QMSR Industry GMPs 111 GMP Publications & The Auditing

Name: 21 CFR 11, 210/211, 606, 820 - Electronic Records with Drug, Blood and Device QMSR Industry GMPs 111 GMP Publications & The Auditing
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Description

GMP Publications & The Auditing Group

EU & ICH GMP Handbook with the new ICH Q7 GMP Auditor's Check List

Registration

The GMP 210/211 regulations address issues including recordkeeping

21 CFR 11, 210/211, 606, 820 - Electronic Records with Drug, Blood and Device QMSR Industry GMPs 111 GMP Publications & The Auditing11, 210,211, 606, 820 Blood QMSR GMPs

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