EU CTR terminology

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Across
  1. 2. Clinical trial directive
  2. 4. Annual safety reporting
  3. 6. clinical trial regulation
  4. 7. Business Intelligence
  5. 8. Ethics Committee
  6. 9. investigational medical product
  7. 10. member state
  8. 11. identity access management
  9. 13. Non substantial modification
  10. 15. Anatomical Therapeutic Chemical Code
  11. 17. european economic area
  12. 18. Application Programming Interface
  13. 20. European Union Clinical Trial Number
  14. 21. Substantial Modification
  15. 22. Reporting Member state
Down
  1. 1. european commission
  2. 3. Draft Assessment report
  3. 5. Request for information
  4. 6. Clinical trial information system
  5. 8. european medicines agency
  6. 10. Member state concerned
  7. 11. investigational medical product dossier
  8. 12. Market authorisation holder
  9. 14. National competant authority
  10. 16. Clinical trial application
  11. 17. European Union Clinical trial Regulation
  12. 19. extended EudraVigilance Medicinal Product Data Dictionary
  13. 23. market authorisation