IVDR Resources
Navigating IVDR: Key Deadlines and Compliance for EU IVDs
The EU’s In Vitro Diagnostic Regulation (IVDR) is now in effect, replacing the former IVDD. With stricter requirements and tighter oversight, IVD manufacturers must adapt quickly to maintain market access.
Transition timelines vary by device class:
- Class D: Until Dec 31, 2027
- Class C: Until Dec 31, 2028
- Class B & A Sterile: Until Dec 31, 2029
- Class A Non-Sterile & New Devices: No extension
Missed deadlines mean lost revenue and limited patient access.
ELIQUENT Life Sciences brings regulatory clarity to this complex shift. Our expert team supports you with transition planning, documentation updates, and Notified Body engagement – ensuring your IVDs remain compliant and market-ready.
MicroLearnings
Short on time? ELIQUENT’s MicroLearnings are designed to deliver key information in a quick, engaging, and easily digestible format. These short, high-impact lessons are perfect for busy professionals who need relevant, practical insights without the time commitment of traditional training.
Explore our Navigating IVDR micro-learning and build your expertise, one lesson at a time!
Discover What’s Changing
& Why It Matters
This micro-learning is perfect for regulatory, quality, and compliance professionals looking for a concise, practical breakdown of how to navigate IVDR. Stay informed and stay compliant – watch now!
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