Approval service
We co-ordinate and implement national and international approval processes for drugs and medicinal products. In addition to dealing with local, centralised and non-European processes, we also carry out US approval processes.


Approval documentation
We always ensure that our customer dossiers are kept fully up-to-date.
We keep a close eye on dossier status in this respect and check for compliance with regulations. We revise certificates and ensure that documentation is renewed or amended as appropriate.
We take care of adjustments to changed manufacturing conditions – such as equipment adaptation or batch sizes – the implementation of additional manufacturers or active ingredients as well as changes in manufacturer or active ingredient.

If you require more information please consult the following contact.