Part 2 Fees relating to marketing authorisations

United Kingdom

1. 6Fees for specified pharmaceutical applications
2. 7Decentralised pharmaceutical application where the United Kingdom is the reference member State
3. 8Application for a marketing authorisation for an immunological product
4. 9Decentralised immunological application where the United Kingdom is the reference member State
5. 10Application for a marketing authorisation using identical data
6. 11Application for a provisional marketing authorisation
7. 12Application for a marketing authorisation relating to a parallel import
8. 13Application for a variation
9. 14Application for a variation to a marketing authorisation that has been issued in other member States
10. 15Application for an extension to a marketing authorisation
11. 16Decentralised application for an extension where the United Kingdom is the reference member State
12. 17Provision of information relating to the recognition of a United Kingdom marketing authorisation
13. 18Application for the renewal of a national marketing authorisation
14. 19Application for the renewal of a marketing authorisation granted in more than one member State
15. 20Registration of a homeopathic remedy
16. 21Annual fees for marketing authorisations
17. 22Auditor’s certificate
18. 23Late payment of annual fees