# Commission Regulation (EC) No 1662/95 of 7 July 1995 laying down certain detailed arrangements for implementing the Community decision-making procedures in respect of marketing authorizations for products for human or veterinary use, Introduction: Introductory text

Extent: E+W+S+N.I.

Commission Regulation (EC) No 1662/95
of 7 July 1995
laying down certain detailed arrangements for implementing the Community decision-making procedures in respect of marketing authorizations for products for human or veterinary use
THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Having regard to Council Regulation (EEC) No 2309/93 of 22 July 1993 laying down Community procedures for the authorization and supervision of medicinal products for human and veterinary use and establishing a European Agency for the Evaluation of Medicinal Products, and in particular Articles 10 (3) and 32 (3) thereof,
Whereas under Regulation (EEC) No 2309/93 the Commission is required to adopt the provisions necessary for the purposes of the written procedure in Articles 10 (3) and 32 (3) thereof;
Whereas the measures laid down in this Regulation are in accordance with the opinion of the Standing Committee on Medicinal Products for Human Use and the opinon of the Standing Committee on Veterinary Medicinal Products,
HAS ADOPTED THIS REGULATION:

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Source: https://www.legislation.gov.uk/eur/1995/1662/introduction (the official version)
Page: https://openlegislation.uk/eu-regulation-1995-1662/introduction
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.