My practice as a medical device consultant involves helping manufacturers navigate their complex obligations regarding the regulatory compliance of their products. I work with our clients primarily on the preparation of their technical documentation and manufacturing process validation, in order to obtain and maintain marketing approval of their medical devices.
I joined nexialist in early 2015, after receiving my PhD in Physiology, with a specialisation in hypertension and arterial stiffness, from Macquarie University in Sydney, Australia. I also completed a Master of Science in Biomedical Engineering at the University of Calgary, and a Manufacturing Engineering degree from the University of Ontario Institute of Technology in my hometown of Oshawa, Canada.