Constantly evolving legislation poses continuous challenges to those who want to combine safety, legality and profit in an economic sector as delicate as it is essential for the society.

We follow the regulatory profiles of drugs and medical devices from a civil, administrative and Community perspective. Particular attention is paid to innovative products and their forms of testing, dissemination and use, as well as to products and devices intended for well-being and not specifically medicinal.

We are familiar with the problems of healthcare facilities, with a particular focus on the issues, regulatorily complex, of medical responsibility.