Medidee is delighted to offer a 1-hour FREE regulatory and clinical check-up with our experts on Tuesday, December 15.

The event will be completely ONLINE.

It is dedicated to Medtech companies (Medical Device and In-Vitro Diagnostic) that may have questions related to the classification of their medical device / In-Vitro Diagnostic or that are questioning the classification of their products as medical devices, the conformity assessment route or the requirements in terms of clinical evidence.

Example of topics that might be covered:
• Classification strategy (under MDD/IVDD and MDR/IVDR) of a complex systems, borderline products
• Clinical evaluation requirements of innovative IVD devices
• Conformity assessment route and the context of Covid-19 crisis
• Evaluating your regulatory positioning
• Confirming or building a safe plan including quality and clinical aspects.

Book your hour NOW!
Any question? Please send an email to Eric Santos (eric.santos(at)medidee.com).