IVDR Survival Guide: Know The 4 Main Challenges And How To Overcome Them

With the positive aim of increasing patient safety, the In Vitro Diagnostic Regulation (IVDR) has fundamentally changed the way in vitro diagnostics (IVD) are regulated in the EU. The depth of expectations for review and documentation have increased substantially. As a result, IVD sponsors are having to adapt to a daunting set of regulatory updates.
This webinar will walk through the four primary challenges to IVDR conversion and provide solutions to simplify and de-stress the process so that IVD manufacturers can approach deadlines with more confidence and avoid having products pulled from the market.

Topics addressed:

New IVDR product classification system
Under the new IVDR, a four-class system replaces the old in vitro diagnostic medical devices directive (IVDD) two-class system. Significantly more products fall into the higher risk groups. What are the most notable new rules and modifications to existing rules? How open are they to interpretation? How do you determine what you need to do differently for compliance now?

Dramatic increase in Notified Body (NB) oversight
It’s estimated that, under the new system, the proportion of products requiring NB oversight will increase from 20 percent to 80-90 percent. How will this affect the level of scrutiny on products old and new, the conformity assessment criteria and the level of documentation required?

Combined pressures creating a NB bottleneck
Just as demand is up, the number of NBs has diminished. Excessive demand, the Consolidated NB initiative, increased training requirements and COVID-19 have created a perfect storm making NB evaluations a rare commodity. What do you do when you need one, but the wait time exceeds your product registration date?

Clinical evidence and performance requirements
Whereas in the past, clinical evidence was not needed, IVD manufacturers now need to show a legitimate level of product performance. But what is acceptable evidence and what isn’t for the different classes of devices? What paperwork is needed? When and how must you perform a complete clinical study?