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