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  • Regulatory Rapporteur - April 2025
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    The Organisation for Professionals in Regulatory Affairs
  • Regulatory Rapporteur - April 2025
  • Pharmaceuticals
      • Artificial intelligence
      • ATMP
      • Biologics
      • Chemistry, manufacturing and controls
      • Clinical trials
      • Non-clinical development
      • Oncology
      • Product information
      • Regulatory procedures
    • RR-April-2025-half-cover
      April 2025 – Contents
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      Africa and the MENA region: Opportunities for growth
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      March 2025 – Contents
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    • RR-Nov-2024-Half-Cover
      November 2024 – Contents: Veterinary medicines sessions
    • SUSIMPERATIVE_compressed
      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
    • RR-Nov-2024-Half-Cover
      November 2024 – Contents: Medical devices/IVDs sessions
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      MHRA provides guidance to streamline safety communication
    • Chimwemwe Chamdimba
      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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      RegRapPod − InConversation with Ivo Claassen
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      Africa and the MENA region: Opportunities for growth
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      Data and AI: Readiness, research and real-world impact
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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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Combination Products Stories

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    What can past decision-making data tell us about how the FDA will make future combination product categorisation decisions?

    2022-05-26T11:04:00+01:00

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    Practical insights into the recent EU MDR framework

    2022-04-18T13:18:00+01:00

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