Regulatory Rapporteur January 2026 – Contents
Navigating complexity: Regulation at the interface of innovation, technology and confidence
Overview of the regulatory and development landscape for brain-computer interfaces in neurodegenerative disease treatment
Regulatory challenges and key considerations in the development of radiopharmaceuticals
Demystifying complex generic products: Regulatory pathways and characterisation
Empowering digital innovation in CMC: A framework for regulatory readiness and confidence
The evolving role of the regulatory professional in the age of Artificial Intelligence
2025 UK MDR Regulatory Conference: Meeting report
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MHRA invites Call for Evidence to assess AI regulation
This industry news update explains the reason for the MHRA’s Call for Evidence for AI regulation and provides guidance.
FDA and EMA publish guiding principles of good AI practice in drug development
This industry news updates shares the ten principles of best practice for AI.
Saudi FDA vision to be a leading regulator includes updating guidance on combination products
This industry news updates shares Saudi FDA’s updated guidance for combination products.
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EC proposes regulation to simplify rules on medical and in vitro diagnostic devices
This industry news update shares the EC’saim to simplify medical and IVD device rules through a new proposal.
The VMD changes how it calculates adverse events incidents for animals
This industry news update shares the VMD’s changes to how it calculates adverse events, which has now taken full effect.
DARWIN EU reaches more than 100 research studies
This industry news update shares a major milestone for DARWIN EU that has reached more than 100 research studies.
EMA launches #ItTakesATeam campaign to address medicine shortages
This industry news update explains the #ItTakesATeam campaign which aims to raise awareness of medicine shortages.
RegRapPod − InConversation with Zohra Nasir and Aksa Rahman
InConversation talks careers with Zohra Nasir and Aksa Rahman
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