lexiara

2.

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 person responsible for placing on the market a medicinal product referred to in Part B of the Annex may request that authorization to place the medicinal product on the market be granted by the Community in accordance with the provisions of this Regulation.

· All articles ·

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