Chapter 1 - MDR can be colonized

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Across
  1. 1. Abbreviation for Clinical Investigation Plan
  2. 3. Abbreviation for International Standard Organization
  3. 6. Someone responsible for ensuring compliance within the manufacturer in the EU
  4. 8. The electronic database holding information on medical devices
  5. 9. Overarching principle for device approval
  6. 11. Devices designed to replace or compensate for a missing body part
  7. 12. Observing devices for performance and safety.
  8. 13. The document replacing the Medical Device Directive in the EU
Down
  1. 1. Mark demonstrating compliance with EU standards
  2. 2. Phase involving monitoring of devices after sales
  3. 4. The UK leaving the EU, impacting MDR compliance
  4. 5. A systematic and independent examination of conformity
  5. 7. The process of identifying and assessing potential risks
  6. 10. An organization designated to assess conformity
  7. 11. Abbreviation for post-market surveillance