Application for UK marketing authorisation Application for UK marketing authorisation

1. 49Application for grant of UK marketing authorisation or parallel import licence
2. 50Accompanying material
3. 50ARequirement for certain applications to include results of paediatric investigation plan
4. 50BAgreement and modification of paediatric investigation plan
5. 50CDeferral of initiation or completion of measures in paediatric investigation plan
6. 50DWaiver of production of information in a paediatric investigation plan
7. 50EApplication for paediatric use marketing authorisation
8. 50FOther applications including paediatric indications
9. 50GApplications relating to orphan medicinal products
10. 50HApplications relating to advanced therapy medicinal products
11. 50IApplications relating to conditional marketing authorisations ...
12. 50JApplications in relation to medicinal products containing or consisting of genetically modified organisms
13. 50KApplications relating to POC medicinal products
14. 51Application for UKMA(NI) relating to generic medicinal products
15. 51AApplication for UKMA(GB) relating to generic medicinal products
16. 51BApplication for UKMA(UK) relating to generic medicinal products
17. 52Application for UKMA(NI) relating to certain medicinal products that do not qualify as generic etc
18. 52AApplication for UKMA(GB) relating to certain medicinal products that do not qualify as generic etc
19. 52BApplication for UKMA(UK) relating to certain medicinal products that do not qualify as generic etc.
20. 53Application for UKMA(NI) relating to similar biological medicinal products
21. 53AApplication for UKMA(GB) relating to similar biological medicinal products
22. 53BApplication for UKMA(UK) relating to similar biological medicinal products
23. 54Applications relating to products in well-established medicinal use
24. 55Applications relating to new combinations of active substances
25. 56Applications containing information supplied in relation to another product with consent
26. 57Obligation to update information supplied in connection with application
27. 57AObligation to update information supplied in connection with parallel import licence application