Suzanne Halliday

Suzanne Halliday is an experienced regulatory professional with a robust background in the medical devices sector, currently serving as Vice President of Regulatory at BSI since June 2004. Key responsibilities include leading internal and external training for Medical Device Directives, conducting audits for CE marking and ISO 13485, and overseeing compliance activities in multiple countries including Canada, the USA, Japan, Taiwan, and Australia. Previously, Suzanne has held various roles at BSI, including Director of Regulatory Compliance and Team Leader for Orthopaedic & Dental Devices, where leadership involved managing teams and ensuring compliance for over 200 global clients. Suzanne has also contributed to the field as a Research Coordinator at the Royal Children's Hospital and as a Project Manager at the National Institute of Advanced Industrial Science. Educational qualifications include a D.Phil in Engineering from the University of Oxford and both an MSc and BSc from the University of Waterloo.