Date: 22 January 2026
Time: 16:00 - 17:00 CET | 10 - 11 am EDT
Location: Virtual
Introduction
The European Commission has proposed a revision to IVDR 2.0, aimed at addressing implementation challenges that have arisen since the original IVDR came into force. The draft seeks to refine conformity assessment timelines, enhance coordination among notified bodies and authorities, and alleviate administrative burdens for manufacturers. The proposal is now under consideration by the European Parliament and Council as part of the EU’s legislative process.
This webinar brings together leading experts in EU regulatory affairs and diagnostics compliance to help you understand what’s in the IVDR 2.0 draft and what it could mean for your organisation. We’ll highlight the key proposed changes, discuss practical implications for manufacturers and stakeholders, and provide insights to help you plan for future regulatory developments in the EU diagnostic market.
The webinar consists of a 15-minute presentation, a 30-minute panel discussion, and a 15-minute live Q&A session. Questions for the Q&A session can be submitted through the registration form, emailed to marketing@qservegroup.com, or asked during the webinar.
More information about the agenda and speakers will be added soon.