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GMP Publications - Code of Federal Regulation Handbooks by the FDA

Blood

21 CFR 11, 606 - Electronic Systems with Blood Industry GMPs
21 CFR 58, 606 - Good Laboratory Practice for Blood Industry
21 CFR 606 - Blood Industry
ICH Q2(R2) and ICH Q14 Analytical Validation
EU cGMPs for ATMP - 2018: Guidelines on Good Manufacturing Practice Specific to Advanced Therapy Medicinal Products
Parts 11, 606 and 1271 - Blood Cell & Tissue GMPs
Parts 11, 606 and 1271 - Blood, Cell & Tissue with Annex 14
In Vitro Diagnostics Master Handbook
Title 21 CFR Parts 1 - End Nine Volume Set
example: 211, ISBN, Drug, GMP, Etc. - Press Enter
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