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Since ChatGPT’s debut in November 2022, large language models (LLMs) have demonstrated enormous transformative power in various industries, including healthcare and medical devices.
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Join industry leaders, regulatory professionals and Qserve Expert Gert Bos at MedCon 2026 in Columbus, Ohio on Apil 22-24.
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Join Oliver Schaer and Bingshuo Li on 21-23 April at DMEA 2026 in Berlin and explore practical insights on Digital Health.
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The transition to IVDR is entering its final phase, and the clock is ticking for Class C IVD manufacturers, as Notified Body assessment is now required.
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Turning clinical data into a convincing benefit-risk narrative is the ultimate exercise in storytelling. It must be written with the Notified Body’s reviewers in mind.
Join Gert Bos and Bingshuo Li at TOPRA Symposium 2026 and explore practical insights on improving EU MDR and shaping its future.
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Learn about the roles, responsibilities and legal requirements of a U.S. FDA Agent. Expect to read about compliance implications and common misconceptions.
Companies that import or distribute medical devices in Canada must obtain a Medical Device Establishment Licence (MDEL).
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Learn where Medical Device Start-Ups go wrong and how to avoid these pitfalls.