21 CFR 11, 58, 210/211, 600, 601, 610, 820 - Multi-US GMPs and complaint handling

and complaint handling

ICH Q7 API Auditor's Checklist                                                                                                 Note:

Includes Annex 11 Computerized Systems and Annex 15 Qualification and Validation

Part 58 - Good Laboratory Practice

21 CFR 11, 58, 210/211, 600, 601, 610, 820 - Multi-US GMPs and complaint handlingMulti 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