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  • Regulatory Rapporteur - February 2026
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    The Organisation for Professionals in Regulatory Affairs
  • Regulatory Rapporteur - February 2026
  • Pharmaceuticals
      • Artificial intelligence
      • ATMP
      • Biologics
      • Chemistry, manufacturing and controls
      • Clinical trials
      • Non-clinical development
      • Oncology
      • Product information
      • Regulatory procedures
    • Half page-REGRAP-ISSUE 23-1-January 2026
      Regulatory Rapporteur January 2026 – Contents
    • AdobeStock_921561253_cover
      Navigating complexity: Regulation at the interface of innovation, technology and confidence
    • AdobeStock_521699095
      A year of change for the US FDA: An update on notable pilots and programmes
  • Veterinary
    • Jana Schalansky
      November 2025 – Contents: Veterinary medicines sessions
    • RR-June-2025-half cover _masthead
      June 2025 – Contents
    • June cover image licensed
      Veterinary medicines: Translating regulation into practice
    • RR-Nov-2024-Half-Cover
      November 2024 – Contents: Veterinary medicines sessions
  • Medical devices
      • Combination products
      • In-vitro diagnostics
      • Software
      • Artificial intelligence
    • WEARABLES_main image
      Wearable technology: The fine regulatory line between health and wellness
    • REQUEST_main image
      Navigating regulatory scrutiny: An analysis of requests for information in EU combined clinical trials
    • RISK_main image
      Reckoning with risk: Navigating MedTech innovation
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    • DIN SPEC 91509_image
      DIN SPEC 91509: A milestone for structured, digital medical device documentation
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      MHRA points to clinical trial growth and faster assessment routes
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      MHRA invites Call for Evidence to assess AI regulation
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      MedTech in transition: Regulation, risk and real-world impact
    • TOPRA RR JCA 800x533px (6.4 ratio) (002)
      RegRapPod − InConversation with Parexel
    • AdobeStock_921561253_cover
      Navigating complexity: Regulation at the interface of innovation, technology and confidence
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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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