The European Commission launches public consultation on the MDR and IVDR
Medical devices: European Commission issues Q&A on the obligation to notify supply interruptions and discontinuations
UK to implement novel framework for point of care manufacture of medicinal products
EMA adopts reflection paper on the use of Artificial Intelligence (AI)
AI: EMA publishes guiding principles on the use of large language models (LLMs)
Virtual and Digital Health Digest – August 2024
Virtual and Digital Health Digest, May 2024
Getting Ready for the Upcoming Revised EMA CTIS Transparency Rules
EMA publishes first draft of reflection paper on the use of AI in the medicinal product lifecycle
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