The BioMed Alliance is active in a range of different topics in the field of regulatory affairs that are relevant to the work of medical & research societies and the healthcare professionals and researchers that we represent.

Examples of topics that we work on:

  • Medical Devices Regulation & Clinician Involvement in ensuring the safety and effectiveness of medical devices in general
  • In Vitro Diagnostics Regulation & EU regulatory requirements for diagnostic laboratories
  • Health Data Sharing for healthcare and research
  • Provisions for Academic Clinical Trials
  • Health Technology Assesment and the involvement of clinicians and researchers

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