A lack of framework for the validation of in silico models is a major barrier to those software industries engaged in healthcare. The Avicenna Alliance will work towards the creations of such a framework that would allow for maximum market uptake of medical software for pre-clinical and clinical use.
Data Protection and ensuring ease of access to health data for medical research purposes is a key priority of the Alliance.
The Avicenna Alliance is delighted to welcome TÜV SÜD as its newest Partner. TÜV SÜD is a leading Notified Body operating across multiple regulatory territories, including the EU, the United States, the UK, and Asia. With more than 150 years of experience, a presence in 1,000 locations worldwide, and over 30,000 employees, TÜV SÜD is a trusted global partner in testing, inspection, certification, and training solutions.
On 11 and 12 September 2025, our partner iSi Health, Erica Beaucage-Gauvreau and Rocio Castro Vinuelas, organised an excellent symposium in Leuven to bring together key players in the in silico community and promote networking, brainstorming and exchanges.
The Avicenna Alliance is honoured to be invited once again as an Observer to the upcoming International Medical Device Regulators Forum (IMDRF) meeting, which will be hosted by PMDA Japan in Sapporo from September 15–19, 2025. This high-level global event will bring together regulatory authorities, trade organisations, and industry representatives from around the world to address pressing topics in medical device regulation.
Fill in the fields you find below
