How Inclusive Is Digital Inclusion?
To address this question DigiSoc and Ethics@KU Leuven will host an interdisciplinary lunch workshop on 7 May 2026 in Leuven.
To address this question DigiSoc and Ethics@KU Leuven will host an interdisciplinary lunch workshop on 7 May 2026 in Leuven.
The European Medicines Agency (EMA) has announced the successful adoption of ICH M15 (Step 5), establishing a harmonized international framework for planning, evaluating, and communicating Model informed Drug Development (MIDD) evidence.
The U.S. Food and Drug Administration (FDA) has released updated guidance aimed at strengthening how patient perspectives are incorporated into medical device decision-making throughout the total product life cycle.
Three important European consultations are currently open for feedback. These initiatives represent key opportunities to help shape policy and regulatory frameworks impacting research, innovation, and healthcare across Europe.
The U.S. Food and Drug Administration (FDA) has reported the successful achievement of its first-year objectives aimed at reducing animal testing in drug development, representing a notable milestone for the in silico medicine community.
Discover the recently published papers from our community!
Discover the recently published papers from our community!
The VPH Society is preparing to contribute to the upcoming HORIZON-MISS-2026-02-CANCER-01 call under the European Commission Mission on Cancer, and invites interested organisations to get in touch for collaboration.
Over the past months, VPH has been actively involved in a number of project proposals, confirming its role as a trusted partner for high-impact, cross-cutting activities.
The VPH Best Poster Award honours the best poster presentation by a VPH student member at the VPH 2026 Conference. The winner will receive a certificate and a €350 cash prize.
On 18 March 2026, the Food and Drug Administration (FDA) published a new draft guidance titled "General Considerations for the Use of New Approach Methodologies in Drug Development", marking a significant step toward integrating innovative, non-animal methodologies into regulatory decision-making.
On 9 March 2026, the European Medicines Agency (EMA) published the Network Data Steering Group (NDSG) Workplan 2026–2028 outlining a strategic roadmap for strengthening the use of data and AI across the European medicines regulatory network.