How integrated scientific assessment frameworks help build confidence in product safety[i] and performance through real-world evidence and continuous evaluation. While tobacco harm reduction products and medical devices serve fundamentally different purposes and operate within their own distinct reg
“Collaboration needs everyone in the same room working for the patient” How can we bring together different bodies across the NHS, from patients to providers, to improve the spread of innovation and improve outcomes for patients? This is the focus of the Medical Technology Group’s latest report on c
As artificial intelligence creates new opportunities across every part of the medical technology industry, discussions at this year’s Veeva MedTech Summit in Amsterdam highlighted why successful adoption depends on more than technology alone. Data quality, regulatory governance and human expertise w
Chris Whitehouse, a political consultant and expert on medical technology policy and regulation at Whitehouse Communications, and a Trustee of the Bios Centre for bioethics highlights a new survey on mental health digital tech. The Medicines and Healthcare products Regulatory Agency (MHRA) and the N
