# The Medicines (Marketing Authorisations Etc.) Amendment Regulations 2005, Paragraph 3


In the Medical Devices (Consultation Requirements) (Fees) Regulations 1995, in regulation 1 (citation, commencement and interpretation), in paragraph (2), in the definition of “ authorised medicinal product”, after “Council Regulation (EEC) No 2309/93”, insert “or Regulation (EC) No. 726/2004 of the European Parliament and of the Council laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency”.

---
Source: https://www.legislation.gov.uk/uksi/2005/2759/schedule/paragraph/3 (the official version)
Page: https://openlegislation.uk/medicines-marketing-authorisations-etc-amendment-regulations-2005/schedule/paragraph-3
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.