Audit Report with GMP Questionnaire
21 CFR Parts 200, 210.1, 210.2, and 211 – Good Manufacturing Practices (cGMPs) 21 CFR Parts 600, 601, 640, 660, 680, and 1271. ICH Q9 – Quality Risk Management. ICH Q10 – Pharmaceutical Quality Systems. 7341.002 - Inspection of Human Cells, Tissues, and Cellular and Tissue-Based Products (HCT/Ps) (Covers HCT/Ps recovered after 5/25/2005) ................
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