Article 2 Article 2
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 authorization procedure as laid down in Council Directive 65/65/EECf1 or Directive 81/851/EECf2 may, under the terms and conditions provided for in this Regulation, be the subject of a certificate.
Annotations
Footnotes
- f1
-
OJ No L22, 9.12.1965, p.369. Last amended by Directive 89/341/EEC (OJ No L142, 25.5.1989, p.11).
- f2
-
OJ No L317, 6.11.1981, p.1. Amended by Directive 90/676/EEC (OJ No L373, 31.12.1990, p.15).
Notes on Schedule 1
Footnotes
- f1
-
OJ No C114, 8.5.1990, p.10.
- f2
-
OJ No C19, 28.1.1991, p.94 and O.J. No. C150, 15.6.1992.
- f3
-
OJ No C69, 18.3.1991, p.22.