WORLD OF RA

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Across
  1. 2. Name of Germany's Regulatory Agency
  2. 4. Certification to become RA professional
  3. 7. Name of Irish Regulatory Agency
  4. 9. Name of Chinese Regulatory Agency
  5. 10. European Notified Body
  6. 11. USA Clinical Study Application
  7. 13. Japans Commercial Approval submission
  8. 15. USA's Act
  9. 16. Name of USA'S regulatory agency
  10. 17. USA Commercial Approval Submission
  11. 18. European Notified Body
  12. 19. Name of Canadian Regulatory agency
  13. 21. Name of Japan's regulatory agency
  14. 23. Phases of Product Development
  15. 24. Regulatory Affairs
Down
  1. 1. Risk Document
  2. 3. Europe's Regulations
  3. 5. Official US Code of Federal Regulations
  4. 6. Australian regulatory agency
  5. 8. Name of Brazilian Regulatory agency
  6. 9. Clinical Application in Australia
  7. 12. Type of a investigational device exemption
  8. 13. Adverse Event Reporting
  9. 14. Clinical Application in Canada
  10. 16. First Time Human Clinical Use
  11. 17. Risk Document
  12. 20. Europe's Commercial Approval Stamp
  13. 22. Europe's Directive