Table of Contents
Berg Family’s Transformative Donation
Mayo Clinic Berg Innovation Exchange Overview
Unique Philanthropy-Driven Model
Global Healthcare Innovation Strategy
Technology Focus Areas
Future Impact and Expansion Plans
Berg Family’s Transformative Donation
Rochester, Minnesota-based Mayo Clinic has received a groundbreaking $50 million…
Government entities overseeing medication access in New Zealand have been planning their adoption of AI assistants and tools to speed up processes and support decision-making.The New Zealand Medicines and Medical Devices Safety Authority (Medsafe)…
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Looking for real innovation in healthcare IT? In this video from the 2025 MaRS Health Impact event, Colin Hung spotlights five standout startups solving real-world problems in digital health and medical devices—and shares an…
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The National Institute for Health and Care Excellence (NICE) has welcomed the inclusion of a rules-based pathway for medical technologies in the government’s NHS 10 year health plan.
The new approach is intended to…
We reviewed 1016 FDA authorizations of AI/ML-enabled medical devices to develop a taxonomy capturing key variations in clinical and AI-related features. Quantitative image analysis remains the most common application, but its relative proportion has…
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(L to R) MediShout co-founders Ash Kalraiya, chief executive, and Ali Nehme Bahsoun, chief product officer (Credit: MediShout)
Digital Health Pitchfest finalist MediShout has raised $9 million (£6.6m) in Series A funding to accelerate…
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The Medicines and Healthcare products Regulatory Agency (MHRA) has received £1 million in funding for its AI Airlock regulatory sandbox programme.
A regulatory sandbox is a tool which allows businesses to explore and experiment with…
Image Credit: bipartisanpolicy
What You Should Know:
– A new report from the Bipartisan Policy Center (BPC) examines the complex and often fragmented regulatory landscape for health AI tools that fall outside the jurisdiction of the…
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The Medicines and Healthcare products Regulatory Agency’s (MHRA) has announced a major overhaul of how medical devices are regulated in Great Britain as part of a wider transformation of the UK’s medical device regulatory…
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Regulatory agencies, such as the European Commission and the U.S. Food and Drug Administration, are now permitting electronic instructions for use (eIFUs) to be distributed alongside paper instructions for use (IFUs) for medical devices….
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