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GMP Publications - Code of Federal Regulation Handbooks by the FDA

Biological-Blood-Cell

21 CFR 640 - Add. Standards for human blood and blood products
21 CFR 600, 601, 610 - Biologic GMP
21 CFR 1271 - Human Cells, Tissues, and Cellular and Tissue-Based Products
21 CFR 600 - Biological Products: General
21 CFR 601 - Licensing - Biologics
21 CFR 610 - General Biological Products Standards
21 CFR 11, 606 - Electronic Systems with Blood Industry GMPs
21 CFR 660 - Add. Standards for Diagnostic Substances for Lab. Tests
21 CFR 680 - Additional Standards for Miscellaneous Products
ICH Q2(R2) and ICH Q14 Analytical Validation
Parts 11, 606 and 1271 - Blood Cell & Tissue GMPs
Parts 11, 606 and 1271 - Blood, Cell & Tissue with Annex 14
21 CFR 3, 4, 11, 210/211, 820, ICH Q7 - Combination Product GMP Master
In Vitro Diagnostics Master Handbook
GMP Manufacturing Handbook
Title 21 CFR Parts 1 - End Nine Volume Set
example: 211, ISBN, Drug, GMP, Etc. - Press Enter
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