Webinar: What Class C IVD Device Manufacturers Must Do Now to Meet Upcoming Deadlines
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With IVDR transitional eligibility deadlines approaching, many Class C IVD manufacturers are still assessing their evidence and documentation.
To support industry preparation, BSI will be hosting a focused webinar addressing the specific challenges and regulatory expectations for Class C IVD devices.
During the session, we will cover:
- Updated IVDR timelines & milestone impact
- Conformity assessment & clinical evidence requirements
- Performance evaluation & technical documentation expectations
- Submission challenges and how to mitigate them
- Notified body review capacity & planning
- Prioritized next steps for 2026
Designed for regulatory, quality, and product leaders, this webinar will help organizations benchmark readiness and plan proactively for uninterrupted market access.