2023 ANZ QA/RA Month Crossword Puzzle

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Across
  1. 1. Regulatory Authority for Medical Devices in New Zealand
  2. 4. A person or entity who designs, develops, assembles, or processes a finished device
  3. 5. ____ Study. Conducted to determine the shelf life of a product
  4. 10. inspection of processes and records to determine compliance to requirements
  5. 13. pRE=Potential ____ Event
  6. 14. Issued in the report for instances of non-conformance detected during an audit
  7. 15. Dossier of technical information submitted to the regulator for pre-market approval
  8. 16. Removal of product from the market after sale
Down
  1. 2. Non-conforming or returned products must be ____
  2. 3. Corrective and Preventative Action
  3. 6. Required before completing a task
  4. 7. ____ Material is used to directly promote products, services and or software.
  5. 8. Who you must contact before engaging with a new supplier?
  6. 9. Controlled site where products are stored prior to their distribution
  7. 11. Required to import or export certain materials
  8. 12. Regulatory Authority for medical devices in Australia