Regulation (EU) on supplementary protection certificate for pharmaceutical products
The regulation (EC) no. 469/2009 provides for the establishment of supplementary protection certificate for pharmaceutical products and regulates, among others, the terms for granting the certificate, the procedure for submission of application for granted certificate, the certificate results and relevant procedures (such as e.g. the renewal and expiry of the certificate etc.)
Relevant provisions are also included in the national legislation and Regulations for patents.
The said Regulation, which has been published in the Official Journal of the European Union, is provided.