Dr. Alexander Meier and Peter von Czettritz contributed the German Chapter to the inaugural edition of International Comparative Legal Guide – Drug & Medical Device Litigation 2020.
This Comparative Legal Guide is intended to provide global insight into litigation considerations that are of critical importance to the life science industry and practitioners around the world.
In the Germany Chapter, we explore amongst others the regulatory framework for drugs and medical devices in Germany with respect to manufacturing requirements, transactions, clinical trials, data privacy, compassionate use programmes, product recalls as well as lititgation and dispute resolution.
