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.
by Dr. Manja Epping and Christoph Behm
Labelling requirements for medical devices under the new EU Product Safety Regulation
by Dr Paul England and Alina Krukover
by multiple authors
by Lydia Birch and Rebecca Limer
by Geert Theuws