Faculty of Pharmaceutical Science, University of Copenhagen (2008)
Søren Toubro is part of the RA Quality team. Søren has long experience with preparation of CMC documentation for drug substances and drug products in the drug development stage as well as in the post-approval phase, primarily in EU and US. Further, Søren is experienced in preparing and managing applications for a Certificate of Suitability (CEP) for pharmaceutical ingredients with the EDQM.
For more information about Regulatory Affairs Quality Team. click here