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GMP Publications - Code of Federal Regulation Handbooks by the FDA

Laboratory

21 CFR 58 - Good Laboratory Practice
GLP Manufacturing Handbook - 4.5x7.5
GLP Analytical Stability Handbook - 4.5x7.5
GCLP Good Clinical Laboratory Handbook - 4.5x7.5
GLP QSR Master Handbook
GMP International Master Reference Guide
In Vitro Diagnostics Master Handbook
21 CFR 58, 606 - Good Laboratory Practice for Blood Industry
21 CFR 58, 820 - GLP and QSR
ICH M10 Bioanalytical Method Validation
Parts 11, 606 and 1271 - Blood Cell & Tissue GMPs
Parts 11, 606 and 1271 - Blood, Cell & Tissue with Annex 14
Title 21 CFR Parts 1 - End Nine Volume Set
21 CFR 11, 50, 54, 56, 312, 314, ICH E2A, E6(R3) - Good Clinical Practice Handbook
ICH Q2(R2) and ICH Q14 Analytical Validation
example: 211, ISBN, Drug, GMP, Etc. - Press Enter
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