GMP Publications - Code of Federal Regulation Handbooks by the FDA

21 CFR Part 11

21 CFR 11 - Electronic Records with Scope & Application
21 CFR 11 - Electronic Records with Scope & Application and Preambles
21 CFR 11, 210/211 - Electronic Records with Drug GMPs
21 CFR 11, 210/211, 820 - Electronic Records with Drug and Device GMPs
21 CFR 11, 58 - Electronic Records with Scope & App. and GLP
21 CFR 11 - with Scope & Application & Computerized Systems used in Clinical Investigations
21 CFR 11, 203, 205 - PDMA with Electronic Records
21 CFR 11, 820 - Electronic Records with Quality Systems Regulations
21 CFR 11 - Electronic Records with Scope & Application and Part 11 Checklist
21 CFR 11, 111 - Electronic Records with Dietary Supplement GMPs
21 CFR 11, 58, 820 - Electronic Records with GLP and QSR
Electronic Systems Master Handbook 1
Clinical Master Reference Guide
In Vitro Diagnostics Master Handbook
GMP International Master Reference Guide
3 Day On-Site FDA/EU GMP Boot Camp Training Fee - International - 20 free GMP Master Handbooks
Title 21 CFR Parts 1 - End Nine Volume Set
503B Compounding and Packaging
FDA DEA GMP Master Reference Guide
21 CFR 11, 210/211, 820 with Audit Checklists - GMP Auditorís Basic Handbook
Dietary Supplement Master Handbook
GMP - PAT Handbook
3 Day On-Site FDA/EU GMP Training Bootcamp - US - 20 free GMP Master Handbooks
Audit - US
2 Day Drug GMP Bootcamp - US - 20 free GMP Master Handbooks
example: 211, ISBN, Drug, GMP, Etc. - Press Enter
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