GEIGER | NITZ | DAUNDERER Kompetenz Arzneimittelrecht und Medizinproduktrecht


We provide comprehensive advice on the regulatory framework for pharmaceuticals and medical devices.

This comprises the legal qualification of your product, the requirements for its marketability and any issues regarding its import, marketing or sale. We support you in connection with differentation issues, in the communication with federal administrative agencies or ethics committees as well as in drafting contracts, with a specific focus on clinical research and contract manufacturing of pharmaceuticals.

We place specific focus on the specific nature and issues of biochemically manufactured pharmaceuticals, innovative genetic therapies as well as on the connection between regulatory issues and the eligibility of such therapies for reimbursement under social law.