OpenLegislation

Part 3 Grant of a marketing authorisation

United Kingdom

  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. 22AWithdrawal of application for marketing authorisation
  8. 23Marketing authorisations for food-producing species
  9. 24Refusal of a marketing authorisation
  10. 25Publication following the grant , refusal, suspension, variation or revocation of a marketing authorisation
  11. 26Marketing authorisations in exceptional circumstances
  12. 27Provisions of samples and expertise
  13. 28Records and supply of information
  14. 29Duties on the holder of a marketing authorisation relating to an immunological product
  15. 30Control tests
  16. 31Placing on the market
  17. 32Duration and validity of marketing authorisation

Notes on Schedule 1

Textual amendments

F1

Words in Sch. 1 heading inserted (E.W.S.) (31.12.2020) by The Veterinary Medicines and Residues (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1461), regs. 1(2)(b), 4(7)(a)

F2

Words in Sch. 1 heading inserted (N.I.) (31.12.2020) by The Animals (Health, Identification, Trade and Veterinary Medicines) (Amendment) (EU Exit) Regulations (Northern Ireland) 2020 (S.R. 2020/353), regs. 1(3), 10(13)(a)