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
GMP Desk Reference Set
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
Medical Device Quality Systems Manual with 11, 820, QSR Audit Checklist, 7382.845 with QSIT
Electronic Systems Master Handbook 1
US, EU and Japanese GMPs
GMP - PAT Handbook
ICH Q7 with Q7 Auditors Check List
GMP Medical Device Master Reference Guide
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
21 CFR Parts 11, 820 QSR and 830 UDI
Chinese GMPs -SFDA - State Food & Drug Administration P.R. CHINA
3 Day On-Site FDA/EU GMP Boot Camp 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
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