Experts assess EU medical device and diagnostic regulations at RAPS Convergence 2026
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A panel of experts representing the European Commission, industry groups and notified bodies gathered in Charlotte, North Carolina during RAPS Convergence 2026.
The group reviewed the current state of the EU Medical Device Regulation (MDR) and In Vitro Diagnostics Regulation (IVDR) as proposed reforms are considered.
Participants discussed implementation challenges, timelines and potential impacts on manufacturers and the broader healthcare market.
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This writeup was produced by pharmadog from original reporting by raps.
Original headline: “Convergence: Experts review the state of play for MDR/IVDR amid proposed reforms”
read at raps ↗
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