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Medical Devices

21 CFR Part 820 / QMSR - Medical Devices

15 modules, in the sequence the regulation was designed to be learned. Open any module to see what it covers.

  1. 1General Provisions and QMSR ScopeSubpart A · 28 min
  2. 2Quality System RequirementsSubpart B · 32 min
  3. 3Design ControlsSubpart C · 41 min
  4. 4Document ControlsSubpart D · 22 min
  5. 5Purchasing ControlsSubpart E · 27 min
  6. 6Identification and TraceabilitySubpart F · 24 min
  7. 7Production and Process ControlsSubpart G · 38 min
  8. 8Acceptance ActivitiesSubpart H · 26 min
  9. 9Nonconforming ProductSubpart I · 25 min
  10. 10Corrective and Preventive ActionSubpart J · 36 min
  11. 11Labeling and Packaging ControlSubpart K · 27 min
  12. 12Handling, Storage, Distribution and InstallationSubpart L · 23 min
  13. 13RecordsSubpart M · 30 min
  14. 14ServicingSubpart N · 21 min
  15. 15Statistical TechniquesSubpart O · 26 min

Start with the first six, free

The three-day trial opens the first six modules of one series on screen, with no card and nothing to cancel.Start the 3-day trialSee pricing for 21 CFR Part 820 / QMSR