Regulatory Affairs
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.
Description
The Regulatory Affairs Committee oversees the rapidly expanding EU health agenda, with a growing number of regulatory files overlapping and increasingly relying on input from healthcare professionals and researchers for effective implementation. BioMed Alliance acts as a common voice for the whole profession to provide collective input and contribute to evidence-based policy making on a broad range of regulatory files. Areas where the BioMed Alliance is active include health data sharing, Health Technology Assessment, clinical trials and the evaluation of medical devices, IVDs and medicines.
Chair
This Committee is Chaired by Prof. Tom Melvin.
Here are the topics that we work on: