Expert e-publications covering the EU MDR/IVDR, clinical evaluation, regulation of software and AI, environmental issues, combination products, and global market access.
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Trending topics: MDR/IVDR Clinical Software/AI/Digital Health Environment Combinations/Borderlines
Newly added publications
Regulatory Intelligence Pack: AI in MedTech
AI-enabled medical devices are now firmly in scope of multiple regulatory frameworks. This Regulatory Intelligence Pack provides a curated set of high-impact AI insights, designed to offer you clarity and practical considerations. Read More...
£149.00
Use of artificial intelligence in literature screening for regulatory compliance
Discover how AI tools can streamline literature reviews for clinical evaluation Read More...
£50.00
Analysis of the European Commission’s proposal for the revision of the MDR and IVDR
A legal analysis of the European Commission proposal and its impact on certification and clinical strategy Read More...
£69.00
An updated overview of the regulatory requirements for medical devices, including IVDs, in Cuba
Get up to speed on Cuba’s latest regulatory developments, including new provisions covering both medical devices and IVDs, and what they mean for market access and compliance Read More...
£50.00
Spotlight on recent regulatory changes in Uzbekistan
A timely overview of Uzbekistan’s updated regulatory framework, including streamlined approval routes and alignment with international standards Read More...
£79.00
Regulatory Monitor – updating you on legislative changes
Get the latest international regulatory updates from the JMDR May 2026 issue – concise, expert-curated updates to keep you ahead in the medical device industry Read More...
£145.00
Regulatory Intelligence Pack: Middle East & Africa
Expanding into emerging markets requires reliable, practical information that’s often hard to access - this Regulatory Intelligence Pack provides country overviews of key Middle East and African markets Read More...
£235.00
