All combined trials articles
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JournalNavigating regulatory scrutiny: An analysis of requests for information in EU combined clinical trials
This article explores aspects of IVDR and how to implement these during clinical trial processes including submissions.
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ContentsRegulatory Rapporteur February 2026 – Contents
The February issue of Regulatory Rapporteur focuses on MedTech.
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EditorialMedTech in transition: Regulation, risk and real-world impact
This issue is shaped by a unifying theme: how risk, evidence, inclusivity and innovation are being brought to the forefront by evolving regulatory expectations across the medical device lifecycle.