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The transition to IVDR is entering its final phase, and the clock is ticking for Class C IVD manufacturers. Under the IVDR, Class C devices now require assessment by a notified body.
Join Gert Bos and Bingshuo Li at TOPRA Symposium 2026 and explore practical insights on improving EU MDR and shaping its future.
Qserve is a Gold Partner at the European Medical Device Summit 2026. Meet our experts and explore regulatory, QMS, clinical, and training solutions.
Meet Qserve at DIA Europe 2026, Track 6, as Gert Bos discusses innovation and competitiveness in European medical devices and combination products.
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We’re pleased to announce the return of the Qserve MedTech Conference, a must-attend event for MedTech professionals navigating an evolving global regulatory landscape.
Join Qserve at RAPS Euro Convergence 2026! Visit Booth #29 to meet our experts, explore the latest in regulatory affairs, and stay tuned for more details.