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Part 108 - Emergency Permit Control
Packaging or Holding Produce
CGMP for Drugs Auditor’s Check List
EUGMPs-Annex11-15-C-251225
US, EU and Canadian Medical Device Combination QMSR Part 108 - Emergency PermitUS FDA Parts Part 11 Electronic Records Electronic Signatures (ERES) Part 50 Protection of Human Subjects Part 54 Financial Disclosure by Clinical Invest. Part 56 Institutional Review Boards Part 801 Labeling Medical Devices Part 803 Medical Device Reporting Part 806 Medical Devices; Reports of Corrections & Removals Part 807 Establishment Registration and Device Listing for Manufacturers & Initial Importers of Devices Part 812 Investigational Device
