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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
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