Yossi Cohen, Physician Executive at InterSystems argues that meeting England’s 2027 health targets requires upgrading shared care records to allow true cross-organisational co-authorship. He recommends piloting this collaborative, patient-inclusive approach with small cohorts before scaling it acros
How is computational modelling transforming R&D efficiency in medical device manufacturing? Ahead of Med-Tech Expo next week, we sat down with Simon Derry, Senior Application Engineer at COMSOL, Inc., to preview his conference session, titled: “Simulation and Modelling of Medical Devices.” Computati
“Developments In Printed Circuit Board Technology for Future Medical Electronics” We spoke to Dr. Manuel Martina, a Consultant for Microsystems Technology with DYCONEX, for a preview of his upcoming conference session at Med-Tech Expo, where Manuel will explain how to push the boundaries of miniatur
Jeff Houtz, global sr. product manager at QuidelOrtho, explores the challenges women face in the diagnosis of thyroid conditions, including biases in diagnosis and screening barriers. Why do thyroid conditions continue to be so difficult to diagnose, particularly in women? So, I think probably the e
“Speed and agility isn’t necessarily about moving faster—it’s about learning earlier.” In our latest Meet the Speakers interview, Samuel Guest, Global Product Manager at Protolabs, challenges the common belief that manufacturing is the primary barrier to MedTech progress. Instead, he points to late-
With average time to endometriosis diagnosis in the UK now 9 years 4 months, Hermione Blakiston from Sagentia Medical explains how clinical adoption of menstrual blood as a diagnostic sample could help accelerate the care pathway. The gold standard for diagnosing endometriosis – laparoscopy – requir
“What Comes After the Single Use for MedTech” In another instalment of our 2026 “Meet the Speakers” series, Editor Oliver Johnson caught up with Millie Marriott Webb from After the Single Use, a research project led by The University of Edinburgh, for a preview of her upcoming conference session at
Good Manufacturing Practice (GMP) compliance is fundamental for laboratories operating in regulated industries such as pharmaceuticals, medical devices, medicinal cannabis and reduced-risk nicotine products. Ensuring data integrity, maintaining traceability and enforcing controlled processes are all
“Even if you don’t realise your device is considered radio equipment, it probably is.” In our latest Meet the Speakers interview, Alexander Toohie, Technical Solution Manager at Element Materials Technology, previews his Med-Tech Expo conference session, where he will shed light on a frequently over
“Blurred Lines: When Medical Devices Fall Between Regulatory Definitions” In the latest instalment of our Med-Tech Expo 2026 “Meet the Speakers” series, we spoke to Bethany Dean from Taylored Consultancy for a preview of her upcoming conference session at Med-Tech Expo. If you want to navigate the c
Chris Whitehouse, a political consultant and expert on medical technology policy and regulation at Whitehouse Communications, calls for urgent clarification on the approach of England’s NHS supply giant to value-based procurement and warns that government ministers may be being misled. A recent, suc
“Regulatory Strategy as a Growth Lever: What UK and EU Assessors and Investors Expect” We spoke to Benyamin Rahmani, PhD from MedStride for a preview of his upcoming conference session at Med-Tech Expo. If you want to stop viewing regulatory as a “compliance exercise” and start using it as a strateg
