Medical device industry

The medical device industry is a constantly growing area, which sits in the crossfire between regulatory requirements and conditions of civil law.  We advise our clients both in the requirements of product compliance - such as the Medical Device Directive - or the rules of the FDA, and on the realization of contracts with clients and suppliers.  Here, we also look at the prevention of product liability and the defense against claims.
Dealings with the supervisory bodies of the EU's Vigilance System must be considered just as carefully as must the regulations of pharmaceutical and medical device law, when differentiating between medical devices and pharmaceuticals.
Protection of intellectual property, analysis of issues of parallel import and strategy against counterfeit products completes our spectrum of competence.