Dierks + Bohle
Germany (reimbursement) and Europe (regulatory advice for medical device certification).
We are a partnership of attorneys established in 1997 and we primarily practice medical law. Our clients include manufacturers of medical devices, medical practicioners, pharmaceutical companies.
We have a nationwide presence. Since an increasing number of medical mandates – for instance, in the field of law governing drugs and medical devices – are not confined to national boundaries, we work with law firms based in other European countries which specialize in similar fields.
Areas of regulatory/reimbursement support:
Market entry and market access strategy, clinical trials, certification and contracts, applications and reimbursement strategy and negotiation. Our aim is to deliver affordable, high quality, useful and accessible consultation for the members of the hub.