Are you a startup developing a medical device or in-vitro diagnostics product? Are you wondering if market access via the FDA is easier compared to CE certification in Europe? Then this event is for you. We will explain the product classes in the US, show you the different approaches of conformity assessment and share insights about costs and timing. At the end of this workshop, you will understand how to identify your route to the US market and know how to collaborate with the FDA.
Market access to US for medical devices
Basel Area Business & Innovation & Effectum Medical AG
Participation is free, however registration is required before August 29th 2023.