GMP Publications - Code of Federal Regulation Handbooks by the FDA

21 CFR Parts 210 - 211 Drug GMP Combinations

21 CFR 210/211 - Drug GMPs
21 CFR 11, 210/211 with Keyword Index
21 CFR 210/211 with Keyword Index
21 CFR 11, 210/211, 820 - Electronic Records with Drug and Device GMPs
21 CFR 11, 58, 210/211, 600, 601, 610, 820 - Multi-US GMPs
21 CFR 11, 210/211, 820, ICH Q7 - Good Manufacturing Practice Handbook
21 CFR 11, 210/211 - Electronic Records with Drug GMPs
21 CFR 203 - Prescription Drug Marketing
21 CFR 205 - Guidelines for Licensing of Wholesale Drug
21 CFR 11, 203, 205 - PDMA with Electronic Records
21 CFR 11, 210/211, 820 with Audit Checklists - GMP Auditorís Basic Handbook
GMP - PAT Handbook
21 CFR 210/211 with Drug Preambles
Japanese GMP for Drugs and Quasi-drugs - 2005
2 Day Drug GMP Bootcamp - US - 20 free GMP Master Handbooks
3 Day On-Site FDA/EU GMP Training Bootcamp - US - 20 free GMP Master Handbooks
US, EU and Japanese GMPs
US and Canadian GMPs with ICH Q7, Q8(R2), Q9, Q10
21 CFR 4 - cGMP for Combination Products
Audit - US with 2 day Training
21 CFR 3, 4, 11, 210/211, 820, ICH Q7 - Combination Product GMP Master
3 Day On-Site FDA/EU GMP Boot Camp Training Fee - International - 20 free GMP Master Handbooks
503B Compounding and Packaging
FDA DEA GMP Master Reference Guide
Audit - US
21 CFR 11, 58, 820 - Electronic Records with GLP and QSR
GMP International Master Reference Guide
Title 21 CFR Parts 1 - End Nine Volume Set
example: 211, ISBN, Drug, GMP, Etc. - Press Enter
Mix and Match End of Year Special New Books Featured Publication GMP Boot Camp GCP Device GMP GCP-DRUG Featured Publication
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