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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)- Recitals
- 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
- Final