# The Patents (Supplementary Protection Certificate for Medicinal Products) Rules 1992, 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/EEC or Directive 81/851/EEC may, under the terms and conditions provided for in this Regulation, be the subject of a certificate.

---
Source: https://www.legislation.gov.uk/uksi/1992/3162/schedule/1/crossheading/article-2 (the official version)
Page: https://openlegislation.uk/patents-supplementary-protection-certificate-for-medicinal-products-rules-1992/schedule-1/crossheading-article-2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.