We advise businesses on the manufacture, import and distribution of medical devices of all classes. We are very familiar with the challenges confronting our clients with the coming into force of the Medical Devices Regulation and currently the IVDR (Invitro Diagnostic Regulation). Our advice is pragmatic and professional.

We advise on clinical trials and conformity and certification proceedings and draft the various contracts required at the levels of development, manufacturing and distribution. We assist with the proper labelling and marketing of medical devices. In this field we can rely on our competition and drugs advertising law expertise. We support and represent our clients in court proceedings and official complaints. That applies both to the inclusion of medical devices in the catalogue of therapeutic appliances and the accounting vis-à-vis statutory health insurers and statutory health insurance accredited doctors’ associations.