Explain the responsibilities of EMA, competent authorities and notified bodies
Understand differences between pharma and medical device law
Clinical data and evaluation according to MEDDEV 2.7.1
Classification of medical devices and impact on data requirements
Device & drug combination products
Conformity assessment and CE-marking of medical devices
Revision of EU medical device law
Risk management and vigilance
Who should Attend
Senior attendees involved or interested in Experienced professionals and newcomers in pharma and medtech industries.
Past Events
Crash Course in EU Medical Device Law for Pharma Professionals 2015 - 21 May 2015, Basel, Switzerland (51412)
Important
Please, check "Crash Course in EU Medical Device Law for Pharma Professionals" official website for possible changes, before making any traveling arrangements
Event Categories
Health & Medicine: Medical device, Medical laboratories, Medical technology, Pharma
