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Regulation (EC) No 816/2006 of the European Parliament and of the Council of 17 May 2006 on compulsory licensing of patents relating to the manufacture of pharmaceutical products for export to countries with public health problems article 6 CELEX: 32006R0816 Application for a compulsory licence
1. Any person may submit an application for a compulsory licence under this Regulation to a competent authority in the Member State or States where patents or supplementary protection certificates have effect and cover his intended activities of manufacture and sale for export. 2. If the person applying for a compulsory licence is submitting applications to authorities in more than one country for the same product, he shall indicate that fact in each application, together with details of the quantities and importing countries concerned. |
Regulation (EC) No 816/2006 of the European Parliament and of the Council of 17 May 2006 on compulsory licensing of patents relating to the manufacture of pharmaceutical products for export to countries with public health problems article 6 CELEX: 32006R0816 3. The application pursuant to paragraph 1 shall set out the following: (a) the name and contact details of the applicant and of any agent or representative whom the applicant has appointed to act for him before the competent authority; (b) the non-proprietary name of the pharmaceutical product or products which the applicant intends to manufacture and sell for export under the compulsory licence; (c) the amount of pharmaceutical product which the applicant seeks to produce under the compulsory licence; (d) the importing country or countries; (e) where applicable, evidence of prior negotiation with the rights-holder pursuant to Article 9; (f) evidence of a specific request from: (i) authorised representatives of the importing country or countries; or (ii) a non-governmental organisation acting with the formal authorisation of one or more importing countries; or (iii) UN bodies or other international health organisations acting with the formal authorisation of one or more importing countries, indicating the quantity of product required. |
Regulation (EC) No 816/2006 of the European Parliament and of the Council of 17 May 2006 on compulsory licensing of patents relating to the manufacture of pharmaceutical products for export to countries with public health problems article 6 CELEX: 32006R0816 4. Purely formal or administrative requirements necessary for the efficient processing of the application may be prescribed under national law. Such requirements shall not add unnecessarily to the costs or burdens placed upon the applicant and, in any event, shall not render the procedure for granting compulsory licences under this Regulation more burdensome than the procedure for the granting of other compulsory licences under national law. |