21 CFR 11, 58, 210/211, 600, 601, 610, 820 - Multi-US GMPs Part 58 - Good Laboratory

Part 58 - Good Laboratory Practice

Part 50 Protection of human subjects

Electronic Records and Good Laboratory Practice

Includes Annex 11 Computerized Systems and Annex 15 Qualification and Validation

process validation

21 CFR 11, 58, 210/211, 600, 601, 610, 820 - Multi-US GMPs Part 58 - Good LaboratoryMulti US GMPs US FDA Title 21 CFR Parts: Part 11 Electronic Records Electronic Signatures (ERES) with Scope and Application Part 58 Good Laboratory Practice (GLP) for Nonclinical Laboratory Studies Part 210 211 GMP in Manufacturing, Processing, Packaging or Holding of Drugs and Finished Pharmaceuticals Part 600 Biological Products: General Part 601 Licensing Biologics Part 610 General Biological Products Standards Part 820 Quality Management System