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NEWS
News
Harmonizing the Future: Global Regulatory Perspectives on In Silico Evidence
If we can submit in silico evidence for regulatory approval to the FDA, we still need to rely exclusively on clinical trial result to the rest of the world until regulation are harmonized! Really? Let's ask the question to the regulators.
News
Don’t Miss Our Keynote with Dr. Bassil Akra – 28 April 2026, 2 pm CEST
Dr. Bassil Akra, a visionary leader in European medtech regulation, will reveal how medical device and IVD rules are evolving.
News
Avicenna Days (AAD) 2026
You’re invited… and yes, this party is free.
