Commission Regulation (EC) No 507/2006 of 29 March 2006 on the conditional market... (32006R0507)
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)
- 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)
- Article 1
- Subject matter
- Article 2
- Scope
- Article 3
- Requests or proposals
- Article 4
- Requirements
- Article 5
- Specific obligations
- Article 6
- Renewal
- Article 7
- Marketing authorisation not subject to specific obligations
- Article 8
- Product Information
- Article 9
- Periodic safety update reports
- Article 10
- Agency advice prior to marketing authorisation application
- Article 11
- Guidelines
- Article 12
- Transitional provision
- Article 13
- Entry into force
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