News

BioMed Alliance attends the EU Health Coalition Summit 2025
On 28 January, the BioMed Alliance team attended the EU Health Coalition Summit in Brussels. The event brought together the partners of the Coalition to listen on important discussions surrounding t...

New recommendations: How the Healthcare & Research Community Can Help Build the European Health Data Space
The BioMed Alliance has published a new policy document, How the Healthcare & Research Community Can Help Build the European Health Data Space, focusing on crucial recommendations for shaping and...

New Policy Recommendations focus on Key Shortcomings in MDR & IVDR
The BioMed Alliance has released two policy documents which include recommendations of healthcare professionals to address persisting challenges in the implementation of the Medical Device Regulation...

BioMed Alliance hosts Training Day on Regulatory Affairs for Clinicians and Researchers
On 27 November, the BioMed Alliance organized a Training Day for clinicians and researchers on key EU healthy policy files including the Health Technology Assessment (HTA), the Medical Devices Regulat...

Your Expertise Needed: Apply to EMA SAGs and EU MD/IVD Panels
The European Medicines Agency (EMA) is calling for experts to join its Scientific Advisory Groups (SAGs) as part of the upcoming mandate renewal. These advisory groups, managed by the Committee fo...

Annual General Assembly brings medical societies to Brussels
At the end of November, the BioMed Alliance organised 2 days of meetings for its members to discuss EU policies and regulations and ongoing and upcoming activities. A significant number of medical soc...

BioMed Alliance welcomes the introduction of the Q&A of article 10a in the IVD and MD Regulation
We are pleased to welcome the European Commission decision to include the Q&A on Article 10a, "The Information Obligation in Case of Interruption or Discontinuation of Supply of Certain Medical De...

BioMed Alliance Responds to new HTA Consultation
Following the Public Consultation on the draft implementing act on the joint scientific consultations on medicinal products for human use under the Health Technology Assessment (HTA) Regulation, the...

Plans made in haste to change Medical Device Regulations (MDR) risk further neglecting the needs of patients who rely on medical technologies.
Following the recent plenary session of the European Parliament, the BioMed Alliance publishes a new statement sharing its concerns about the debate on accelerating the evaluation of the Medical Devic...

EMA seeks experts for its medical devices expert panels and healthcare professionals working party
The European Medicines Agency (EMA) has launched a call for expression of interest for experts in medical devices and in-vitro diagnostics (IVDs) as part of the EXPAMED initiative. The purpose is to g...

Join the first BioMed Alliance training day on regulatory affairs
Have you always wanted to get more in-depth knowledge on how EU health policy making works and how you can have an impact? Then you should join the first BioMed Alliance training day on 27 November, w...

Join the BioMed Alliance Workshop on how the healthcare & research community can help build the European Health Data Space
BioMed Alliance is organising a public workshop on 'Building Bridges: how the healthcare & research community can help build the European Health Data Space' taking place on 15 October from 14:...