Dario Pirovano

Consultant Regulatory Affairs

Dario Pirovano been a consultant for regulatory affairs with Eucomed since 2002. He worked in the European Commission for 4 years, where he contributed to the drafting and negotiating of the 90/385 /EEC and 93/42/EEC directives.

Dario has over 30 years experience in medical technology as designer and regulatory affairs expert. In 1995 he founded Pirovano Management SPRL, a consulting firm advising manufacturers, Notified Bodies and authorities in regulatory matters relating to medical technology.

Dario can be considered the historical memory of the development of medical devices regulation in Europe. He holds a Doctorate in Engineering from the Politecnico di Milano. An Italian national, Dario is fluent in French and English.

1 blog from the author

Access Regulation

Posted on 07.04.2009

More from the DIA EuroMeeting 2009

From 23 – 25 March 2009, the Drug Information Association (DIA) held its annual EuroMeeting in Berlin. During the presentation by Richard Moore, Institute of Nanotechnology, I learned that prescription drugs prove to be ineffective in 30% – 60% of patients1 and that 16% of the drugs approved in the USA are linked to severe […]

By Dario Pirovano Consultant Regulatory Affairs