# Directive 2001/82/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to veterinary medicinal products, Division 7: Mixed marketing authorisation applications

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

Mixed marketing authorisation applications are applications where Part(s) 3 and/or 4 of the dossier consist of safety and efficacy studies carried out by the applicant as well as bibliographical references. All other part(s) are in accordance with the structure described in Part I of Title I of this Annex. The competent authority shall accept the proposed format presented by the applicant on a case-by-case basis.

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Source: https://www.legislation.gov.uk/eudr/2001/82/annex/I/title/III/division/7 (the official version)
Page: https://openlegislation.uk/eu-directive-2001-82/annex-I/title-III/division-7
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.