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