Ewan Kerr-Edwards

Assistant Manager

KPMG in the UK

Ewan has 7 years of experience in regulatory roles developing and implementing global strategies for medical devices and in vitro diagnostic medical devices (IVD).

He has a special interest in technological solutions to regulatory challenges, implementing automated workflows for regulatory documentation and KPI reporting. He has led global medical device regulatory submissions in Europe, USA and China as well as regulatory projects encompassing new product development, labelling and delivery of high-risk medical devices to global markets at speed. He takes a personal interest in software as a medical device, digital health and the use of AI as a diagnostic tool for clinicians, having coded his own machine learning model for prostate cancer diagnosis during his Master’s research project.

  • MSc Precision Medicine

  • BSc Human Biology

  • Precision Medicine

  • Medical Devices

  • In Vitro Diagnostics regulation Artificial Intelligence Regulation

  • Digital Health