- 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 Ortho Clinical Diagnostics on the increased requirements for post market surveillance
- Examine the Medical Device Single Audit Program (MDSAP) with Berlin Heart GmbH