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  • Regulatory Rapporteur - May 2025
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  • Regulatory Rapporteur - May 2025
  • Pharmaceuticals
      • Artificial intelligence
      • ATMP
      • Biologics
      • Chemistry, manufacturing and controls
      • Clinical trials
      • Non-clinical development
      • Oncology
      • Product information
      • Regulatory procedures
    • FDAPLAT final
      ​Navigating the FDA’s platform technology designation: Key insights and best practices for drug manufacturers
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      Navigating orphan drug designation in the EU
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      Prescribing efficiency: Using generative artificial intelligence for pharmacovigilance
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      November 2024 – Contents: Veterinary medicines sessions
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      The sustainability imperative for the healthcare sector
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      New data protection for maximum residue limits
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      EMA platform to monitor use of antimicrobials
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      The EU Medical Device Regulation: Balancing innovation with regulation
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      Medical device regulation: Challenges, innovation and the future
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      November 2024 – Contents: Medical devices/IVDs sessions
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      MHRA provides guidance to streamline safety communication
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      Key milestone reached in African medicines regulation
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      Rui Santos Ivo elected as new Chair of the EMA Management Board
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      Advanced therapies: A maturing regulatory framework
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      RegRapPod − InConversation with Ivo Claassen
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      Africa and the MENA region: Opportunities for growth
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      Streamline medical device compliance with BSI Compliance NavigatorSponsored by The UK's National Standards Body
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      The Olaratumab experience
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      Qualification of stride velocity endpoint in Duchenne Muscular Dystrophy
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