1. Introductory Text

2. Article 1. Definitions

3. Article 2. Scope

4. Article 3. Conditions for obtaining a certificate

5. Article 4. Subject matter of protection

6. Article 5. Effects of the certificate

7. Article 6. Entitlement to the certificate

8. Article 7. Application for a certificate

9. Article 8. Content of the application for a certificate

10. Article 9. Lodging of an application for a certificate

11. Article 10. Grant of the certificate or rejection of the application for a certificate

12. Article 11. Publication

13. Article 12. Fees

14. Article 13. Duration of the certificate

15. Article 13A. Authorisation granted after submission of an application for a certificate

16. Article 13B. Extension of the duration of a certificate

17. Article 14. Expiry of the certificate

18. Article 15. Invalidity of the certificate

19. Article 16. Revocation of an extension of the duration

20. Article 17. Notification of lapse or invalidity

21. Article 18. Appeals

22. Article 19. Procedure

23. Article 19A. Transitional provisions

24. Article 20. Additional provisions relating to the enlargement of the Community

25. Article 21. Transitional provisions

26. Article 21a. Evaluation

27. Article 22. Repeal

28. Article 23. Entry into force

29. Signature

30. 1. ANNEX I

    2. ANNEX -I

       Logo

    3. ANNEX -Ia

       1. Standard form for notification pursuant to points (b) and (c)...

    4. ANNEX II

    5. ANNEX III

       Transitional provisions in relation to applications and certificates for medicinal products for human use concerning the implementation of the Windsor Framework

       1. 1. New applications

       2. 2. Certificates in effect in Northern Ireland

       3. 3. Notification of authorisations

       4. 4. Lapse or withdrawal of certificates

       5. 5. Paediatric extensions