Part 3 Grant of a marketing authorisation

1. 17Time limits
2. 18Place of establishment of applicant
3. 19Procedure
4. 20Products authorised in another member State
5. 21Assessment reports
6. 22Grant of a marketing authorisation
7. 23Marketing authorisations for food-producing species
8. 24Refusal of a marketing authorisation
9. 25Publication following the grant of a marketing authorisation
10. 26Provisional marketing authorisation
11. 27Provisions of samples and expertise
12. 28Supply of information
13. 29Duties on the holder of a marketing authorisation relating to an immunological product
14. 30Control tests
15. 31Placing on the market
16. 32Duration and validity of a marketing authorisation