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  • Regulatory Rapporteur - June 2025
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  • Regulatory Rapporteur - June 2025
  • Pharmaceuticals
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      • Chemistry, manufacturing and controls
      • Clinical trials
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      ​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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      June 2025 – Contents
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      Veterinary medicines: Translating regulation into practice
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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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      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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      ​FDA to replace animal testing with new approach methodologies
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      EMA to address antimicrobial resistance risks from veterinary medicinal products
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      ​MHRA authorises new cancer treatment variation with significantly reduced administration time
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      Advanced therapies: A maturing regulatory framework
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      RegRapPod − InConversation with Ivo Claassen
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