WEBINAR | Are you ready for the IVDR? Regulatory impact and milestones for CE marking

Next month, Dominique Monferrer will hold a webinar aimed to help manufacturers of in vitro diagnostic medical devices to understand the impact of the new In Vitro Diagnostic Regulation (IVDR), the most relevant changes against the current directive and how it will impact both medical devices already in the market and new ones.

Dominique has a PhD in Protein X-ray Crystallography and a BSc in Human Biology. She has over 10 years experience in regulatory affairs and is the Medical Devices team leader at Asphalion. She is an expert in scientific & regulatory assessment in development of medical devices and in vitro diagnostics according to EU and US legal frameworks and in providing regulatory support to manufacturers in CE certification, FDA clearance and life-cycle maintenance of registered products.

This webinar is organised by ECCRT and you can already register on the event page: https://eccrt.com/course_display/are-you-ready-for-the-ivdr-regulatory-impact-and-milestones-for-ce-marking/

More details about this webinar: https://www.asphalion.com/event-calendar/webinar-are-you-ready-for-the-ivdr-regulatory-impact-and-milestones-for-ce-marking/