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Pharmaceutical Industry

Pharmaceutical Industry

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Pharmaceutical Industry

Is the current model fit for purpose?

These are symptoms of a decline of the pre-digital era model of medicinal product development. Our pharmaceutical industry members are those who are committed to moderninsing their product development to create safer and more effective medicinal products.

>Modernisation of the pharmaceutical industry requires a coresponding moderninsation of the way in which medicinal products are brought on to the market and the design of clinical trials. The Avicenna Alliance is working to promote modelling and simulation as a means of addressing the high cost of research and the uptake of in silico methods.

NEWS

News Avicenna Alliance Welcomes the Notified Body TÜV SÜD as a New Partner

Avicenna Alliance Welcomes the Notified Body TÜV SÜD as a New Partner

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.

News The Alliance at the iSi Health Symposium

The Alliance at the iSi Health Symposium

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.

News Avicenna Alliance to Attend IMDRF Meeting in Japan – September 2025

Avicenna Alliance to Attend IMDRF Meeting in Japan – September 2025

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.

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