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21 CFR Part 820 QMSR with ISO 13485 Checklist & Part 11
Regular price $16.95Regular price -
21 CFR Parts 210/211 - Drug GMPs
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21 CFR Part 112 Produce
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Dietary Supplement Master Handbook
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GMP Medical Device Master Reference
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US & EU GMP Regulations with Annex 1 & ICH Q7
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GMP Manufacturing Handbook
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21 CFR Part 111 Dietary Supplements
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21 CFR Part 117 - Food GMPs
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GMP International Master Reference
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Good Clinical Practice Handbook
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2023 NCIMS – Grade “A” Pasteurized Milk Ordinance
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21 CFR 11, 210/211, 820 QMSR - Electronic Records with Drug and Device GMPs
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21 CFR 210/211 with GMP Audit Check List
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US, EU and Japanese GMPs
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21 CFR 3, 4, 11, 210/211, 820, ICH Q7 - Combination Product GMP Master
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21 CFR 11, 110, 117, 120 - Food GMPs
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US and EU GMPs with ICH Q7, Q8(R2), Q9(R1), Q10
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21 CFR 11, 210/211, 700/701 - Cosmetic with "Is It Soap or a Drug"
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21 CFR 11, 210/211, 820 and ICHQ7 with Audit Checklists - GMP Auditor’s Basic Handbook
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21 CFR Parts 600, 601 610 Biologic GMP
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21 CFR 507 - cGMP, Hazard Analysis, and Risk-Based Preventive Controls for Food for Animals
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21 CFR Part 58 - Good Laboratory Practice
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US, Canada GMPs, ICH Q7, Q8, Q9 & Q10
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21 CFR Part 11 with Scope & Application
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Good Clinical Practice – Medical Device
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US FDA, Canadian and European MDR
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21 CFR Part 11, 58 GLP and OECD Series 1 GLP
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US, EU and Canadian Medical Device Combination
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21 CFR 11, 111 - Electronic Records with Dietary Supplement GMPs
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503B Compounding Master Guide
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21 CFR 11, 58, 210/211, 820 - Master GMP Trainer
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21 CFR 11, 210/211 - Electronic Records with Drug GMPs
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21 CFR 11, 58, 210/211, 820, ICH E6(R3) - GMP 2
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21 CFR 11, 58, 210/211, 600, 601, 610, 820 - Multi-US GMPs
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21 CFR 606 - Blood Industry
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