Hear direct feedback and experiences from the FDA on In Vitro registration in USA. Direct your questions to ourexpert panel of Notified Body representatives including BSI, UL, LRQA, TUV SUD, LNE/GMED and TÜV Rheinland. Learn how the change in classifications will impact industry with UL
Hear insights from on the increased requirements for post market surveillance Examine the Medical Device Single Audit Program (MDSAP) with Berlin Heart GmbH