After Authorisation
created: 2008.02.13
updated: 2010.02.09
In the navigation bar on the left you will find:
- National Variations, information about variations in particulars and documents in accordance with sections (§§) 22 – 24 AMG
- Variations, information about variations in particulars and documents in accordance with Variation Regulation (EC) 1234/2008
- Renewals, information about the renewal of marketing authorisation or registration of medicinal products in accordance with §§ 31, 39 AMG and Article 24 of Directive 2001/83/EC and Article 14 of EU Regulation No. 726/2004
- PUMA (Paediatric use marketing authorisation)