SPC Regulation for Medicinal Products
Print this pageRegulation (EC) No 469/2009 of the European Parliament and of the Council of 6 May 2009 concerning the supplementary protection certificate for medicinal products (Codified version) (Text with EEA relevance)
Article 3 - Conditions for obtaining a certificate
Article 4 - Subject matter of protection
Article 5 - Effects of the certificate
Article 6 - Entitlement to the certificate
Article 7 - Application for a certificate
Article 8 - Content of the application for a certificate
Article 9 - Lodging of an application for a certificate
Article 10 - Grant of the certificate or rejection of the application for a certificate
Article 13 - Duration of the certificate
Article 14 - Expiry of the certificate
Article 15 - Invalidity of the certificate
Article 16 - Revocation of an extension of the duration
Article 17 - Notification of lapse or invalidity
Article 20 - Additional provisions relating to the enlargement of the Community
Article 21 - Transitional provisions
Text in force at 01-01-2020. The text can be verified at EUR-LEX. Titles of articles have been added for convenience, but are lacking in the official text, IP-PorTal.
