GMP Publications - Code of Federal Regulation Handbooks by the FDA

GMP Combination Handbooks

21 CFR 11, 210/211, 820, ICH Q7 - Good Manufacturing Practice Handbook
21 CFR 11, 58, 210/211, 600, 601, 610, 820 - Multi-US GMPs
21 CFR 11, 58, 210/211, 820, ICH E6(R1) - GMP 2 Combination Handbook
21 CFR 11, 58, 210/211, 820 - Master GMP Trainer: Guidance Doc. GMPs for the 21st Century & Quality Syst. Approach to GMPs
Canadian GMP Guidelines 2009, Version 2 - Effective March 4, 2011
21 CFR 11, 210/211, 606, 820 - Electronic Records with Drug, Blood and Device QSR Industry GMPs
21 CFR 11, 210/211, 820 with Audit Checklists - GMP Auditorís Basic Handbook
Medical Device Quality Systems Manual with 820 and QSR Audit Checklist
US and Canadian GMPs with ICH Q7, Q8(R2), Q9, Q10
Electronic Systems Master Handbook 1
US, EU and Japanese GMPs
GMP - PAT Handbook
ICH Q7 with Q7 Auditors Check List
21 CFR 11, 58, 820 - Electronic Records with GLP and QSR
3 Day On-Site FDA/EU GMP Training Bootcamp - US
ICH Q7, Q8, Q9, Q10 and Q11
Audit - US with 2 day Training
Chinese GMPs -SFDA - State Food & Drug Administration P.R. CHINA
3 Day On-Site FDA/EU GMP Training Fee - International
21 CFR 3, 4, 11, 210/211, 820, ICH Q7 - Combination Product GMP Master
21 CFR 4 - cGMP for Combination Products
In Vitro Diagnostics Master Handbook
GMP International Master Reference Guide
Audit - US
Title 21 CFR Parts 1 - End Nine Volume Set
example: 211, ISBN, Drug, GMP, Etc. - Press Enter
New Handbooks Mix and Match GCP Device GMP GCP-DRUG Featured Publication GMP Audits and Training Package
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