Article 1
With effect from 1 January 1995, Directive 87/22/EEC is hereby repealed.
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Council Directive 93/41/EEC of 14 June 1993 repealing Directive 87/22/EEC on the approximation of national measures relating to the placing on the market of high- technology medicinal products, particularly those derived from biotechnology
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In force since 1993-08-24, as the publisher states.
Copy read on 2026-11-08. The page it was read from
© European Union, https://eur-lex.europa.eu
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4 provisions
Article 2
Applications for marketing authorizations which have been referred to the Committee for Proprietary Medicinal Products or to the Committee for Veterinary Medicinal Products before 1 January 1995 in accordance with Article 2 of Directive 87/22/EEC and in respect of which the Committee concerned has not given an opinion by 1 January 1995 shall be considered in accordance with Regulation (EEC) No 2309/93.
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Member States shall take all appropriate measures to comply with this Directive with effect from 1 January 1995. They shall forthwith inform the Commission thereof. When Member States adopt these provisions, they shall contain a reference to this Directive or shall be accompanied by such reference at the time of their official publication. The methods of making such a reference shall be laid down by the Member States.
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This Directive is addressed to the Member States. Done at Luxembourg, 14 June 1993. For the Council The President J. TRØJBORG (1) OJ No C 58, 8. 3. 1990, p. 1. (2) OJ No C 183, 15. 7. 1991, p. 145 and OJ No C 150, 31. 5. 1993. (3) OJ No C 269, 14. 10. 1991, p. 84. (4) OJ No L 15, 17. 1. 1987, p. 38. (5) See page 1 of this Official Journal. (6) OJ No L 81, 26. 3. 1988, p. 75. (7) See page 22 of this Official Journal. (8) See page 31 of this Official Journal.
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