Description: Code of Federal Regulations Mini-Handbooks as provided by the Food and Drug Administration FDA. The laws for Pharmaceuticals, BioTechnology, Medical Device and Regulatory Industry. Quality Assurance QA, Blood, Biologics, Drug and Food Industry
gmp (407) fda (361) glp (193) qsr (66) 21 cfr part 11 (23) code of federal regulations (11) part 11 (8) 21 cfr part 820 (3) cfrs (2) 210/211 (2)
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GMP Manufacturing Handbook - Drug, Biologics, Vaccines & APIs - Over 450 pages of Regulations and Guidance. Great for CMOs and GCP Industry.