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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 · European Union

Members of the Management Board, Committee members, rapporteurs and experts shall not have financial or other interests in the pharmaceutical industry which could affect their impartiality. All indirect interests which could relate to this industry shall be entered in a register held by the Agency which the public may consult.

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Source: EUR-Lex (Cellar) · retrieved 2026-11-06 · Text as adopted (Official Journal); later amendments are not incorporated in this text.