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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

The Executive Director shall be the legal representative of the Agency. He shall be responsible: for the day-to-day administration of the Agency, for the provision of appropriate technical support for the Committee for Proprietary Medicinal Products and the Committee for Veterinary Medicinal Products, and their working parties and expert groups, for ensuring that the time limits laid down in Community legislation for the adoption of opinions by the Agency are respected, for ensuring appropriate coordination between the Committee for Proprietary Medicinal Products and the Committee for Veterinary Medicinal Products, for the preparation of the statement of revenue and expenditure and the execution of the budget of the Agency, for all staff matters.

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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.