Commission Regulation (EC) No 507/2006of 29 March 2006on the conditional marketing authorisation for medicinal products for human use falling within the scope of Regulation (EC) No 726/2004 of the European Parliament and of the Council(Text with EEA relevance) (revoked)
Article 1Subject matter
Article 2Scope
Article 3Requests or proposals
Article 4Requirements
Article 5Specific obligations
Article 6Renewal
Article 7Marketing authorisation not subject to specific obligations
Article 8Product Information
Article 9Periodic safety update reports
Article 10Agency advice prior to marketing authorisation application
Article 11Guidelines
Article 12Transitional provision
Article 13Entry into force

Commission Regulation (EC) No 507/2006

of 29 March 2006

on the conditional marketing authorisation for medicinal products for human use falling within the scope of Regulation (EC) No 726/2004 of the European Parliament and of the Council

(Text with EEA relevance) (revoked)

F1. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .