Christoph is a member of the Practice Area Patents Technology & Life Sciences and the Industry Group Life Sciences & Healthcare. His practice focuses on advising national and international pharmaceutical and medical device companies on regulatory aspects and contractual matters, in particular in the field of medicinal product and medical device law.
par Dr. Manja Epping et Christoph Behm
Labelling requirements for medical devices under the new EU Product Safety Regulation
par Christoph Behm
par Bram Nijhof et Nick Strous
par Dr. Lena Niehoff
par Alison Dennis et Dr. Manja Epping
par Victoria Hordern et Dr. Tim Schwarz
par Séverine Bouvy
par Alison Dennis
par Marc Schuler