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21 CFR Parts 210/211 - Drug GMPs
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21 CFR 210/211 with GMP Audit Check List
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21 CFR 210/211 with Keyword Index
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GMP Manufacturing Handbook
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GMP International Master Reference
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Standard Sterile Product Handbook
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EU and US GMPs with Q7 API
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GLP Manufacturing Handbook - 4.5x7.5
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US, EU and Japanese GMPs
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FDA DEA GMP Master Reference Guide
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US and EU GMPs with ICH Q7, Q8(R2), Q9(R1), Q10
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US, Canada GMPs, ICH Q7, Q8, Q9 & Q10
Regular price $19.95Regular price -
21 CFR 210/211 - Drug GMPs-SPANISH
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Pharmaceutical Manufacturers GMP Audit Handbook
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Medical Device Quality Systems Manual with 11, 210/211, 820 and QSR Audit Checklist
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21 CFR Parts 11, 203, 205 - PDMA
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GLP Analytical Stability Handbook - 4.5x7.5
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21 CFR Part 4 Combination Products with 820
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EU cGMPs for ATMP - 2018 Advanced Therapy Medicinal Products
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ICH Q12 Pharmaceutical Product Lifecycle Management
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ICH Q7, ICH Q8(R2), ICH Q9(R1), ICH Q10 and ICH Q12 Combination
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21 CFR 203 - Prescription Drug Marketing
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21 CFR 205 - Guidelines for Licensing of Wholesale Drug
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21 CFR 4 - Regulation of Combination Products
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