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