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  • Regulatory Rapporteur - December 2024
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    The Organisation for Professionals in Regulatory Affairs
  • Regulatory Rapporteur - December 2024
  • Pharmaceuticals
      • Artificial intelligence
      • ATMP
      • Biologics
      • Chemistry, manufacturing and controls
      • Clinical trials
      • Non-clinical development
      • Oncology
      • Product information
      • Regulatory procedures
    • CTR article image final
      Transitioning to the Clinical Trials Regulation: The Roche experience
    • RR-Dec-2024-Half-cover
      December 2024 – Contents
    • RR-Nov-2024-Half-Cover
      November 2024 – Contents: Human medicines sessions
  • Veterinary
    • RR-Nov-2024-Half-Cover
      November 2024 – Contents: Veterinary medicines sessions
    • SUSIMPERATIVE_compressed
      The sustainability imperative for the healthcare sector
    • AdobeStock_537705324
      New data protection for maximum residue limits
    • AdobeStock_294025271
      EMA platform to monitor use of antimicrobials
  • Medical devices
      • Combination products
      • In-vitro diagnostics
      • Software
      • Artificial intelligence
    • RR-Nov-2024-Half-Cover
      November 2024 – Contents: Medical devices/IVDs sessions
    • elabels image_compressed
      E-labelling: revolutionising the labelling landscape
    • AdobeStock_841428142_compressed
      New approach methodologies for the biological safety assessment of medical devices
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    • final alzimer article image
      Increased debate over lecanemab
    • EMA medicine shortages final image
      Use of new EMA platform for monitoring medicine shortages to become mandatory
    • GSK blood cancer article final image
      GSK Blenrep trial shows ‘significant overall survival benefit’of myeloma treatment
  • Commentary
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    • AdobeStock_282144604

      North America:
      Navigating key regulatory updates
    • Michael Kipping
      Improving health outcomes through regulatory excellence
    • AdobeStock_971129498_SMALL
      Chemistry, manufacturing and controls: accelerating development and boosting innovation
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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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All Regulatory Rapporteur articles in November 2024 – Page 2

  • HM6 - RebeccaLumsden
    Journal

    HM6: Artificial Intelligence – How will AI and machine learning tools transform regulatory practice?

    2024-11-08T06:52:00Z

     

  • MD1 -MargarethJorvid
    Journal

    HM5/MD1/IVD1: COMBINE project: A new era of combined clinical trials in Europe

    2024-11-08T06:52:00Z

     

  • HM4 - KatjaPečjakReven
    Journal

    HM4: Electronic product information (ePI) – A digital passport for medicinal product information

    2024-11-08T06:51:00Z

     

  • HM3 - FrancescaButtigieg
    Journal

    HM3: Regulation and innovation – Keeping up with the times (Fireside chat)

    2024-11-08T06:51:00Z

     

  • HM2 ALT - Lada Leyens
    Journal

    HM2: European clinical research ecosystem – How to boost its competitiveness

    2024-11-08T06:51:00Z

     

  • HM1 - SabineHaubenreisser
    Journal

    HM1: Ensuring regulatory excellence

    2024-11-08T06:51:00Z

     

  • RR-Nov-2024-Half-Cover
    Contents

    November 2024 – Contents: Veterinary medicines sessions

    November 2024  |  Vol. 21  |  No. 10

  • RR-Nov-2024-Half-Cover
    Contents

    November 2024 – Contents: Medical devices/IVDs sessions

    November 2024  |  Vol. 21  |  No. 10

  • RR-Nov-2024-Half-Cover
    Contents

    November 2024 – Contents: Human medicines sessions

    November 2024  |  Vol. 21  |  No. 10

  • Michael Kipping
    Editorial

    Improving health outcomes through regulatory excellence

    2024-11-06T12:09:00Z

     

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