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Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency (Text with EEA relevance) · 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 managing all the Agency resources necessary for conducting the activities of the committees referred to in Article 56(1), including making available appropriate scientific and technical support; for ensuring that the time-limits laid down in Community legislation for the adoption of opinions by the Agency are complied with; for ensuring appropriate coordination between the committees referred to in Article 56(1); for the preparation of the draft statement of estimates of the Agency's revenue and expenditure, and execution of its budget; for all staff matters; for providing the secretariat for the Management Board.

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Source: EUR-Lex (Cellar) · retrieved 2026-11-03 · Text as adopted (Official Journal); later amendments are not incorporated in this text.