Article 2

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Any product protected by a patent in the territory of a Member State and subject, prior to being placed on the market as a medicinal product, to an administrative authorisation procedure as laid down in Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use (2) or Directive 2001/82/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to veterinary medicinal products (3) may, under the terms and conditions provided for in this Regulation, be the subject of a certificate.

 

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(2) OJ L 311, 28.11.2001, p. 67.

(3) OJ L 311, 28.11.2001, p. 1.