| Across |
| 4. |
european commission |
| 5. |
clinical trial information system |
| 6. |
clinical trial application |
| 7. |
market authorisation |
| 9. |
Substantial Modification |
| 10. |
clinical trial regulation |
| 11. |
Draft Assessment report |
| 13. |
member state concerned |
| 14. |
european economic area |
| 15. |
identity access management |
| 17. |
extended EudraVigilance Medicinal Product Data Dictionary |
| 19. |
ethics Committee |
| 21. |
request for information |
|
|
| Down |
| 1. |
european Union Clinical Trial Number |
| 2. |
national competant authority |
| 3. |
non substantial modification |
| 8. |
annual safety reporting |
| 10. |
clinical trial directive |
| 12. |
anatomical Therapeutic Chemical Code |
| 13. |
market authorisation holder |
| 14. |
european medicines agency |
| 15. |
investigational medical product |
| 16. |
member state |
| 18. |
european Union Clinical trial Regulation |
| 20. |
business Intelligence |
|
