Regulatory Jurisdictions in Medical Devices

Widgets gadgets doodads and whatsits. The term healthcare innovation is often descriptive of a device or technology. Understanding regulatory requirements specific to devices is crucial to improving health. Join TR talks this week to learn from device experts who can show you which roads to take and which to avoid.

As part of the graduate seminar in the Master of Health Science in Translational Research, Fundamentals of Translational Research, the discussion series is hosted by Faculty of Medicine’s Translational Research Program (TRP) and the five collaborating Departments participating in the development of the Toronto Translational HUB (Department of Psychiatry, Medicine, Imaging, Surgery and Paediatrics).

Geared to an inter-professional community of clinicians, researchers, and trainees, the series is intended to provoke discussion and community building. The Talks, are intended to provide an overview of the health innovation landscape while introducing the ‘tools and competencies’ needed to systematically ‘translate’ science more effectively.

Each seminar in the series is two hours. During the first hour, TRP graduate students will facilitate a discussion among all the panel discussants and audience about Translational challenges and opportunities. During the second hour, each of the discussants will meet in smaller groups with attendees to continue the conversation and network.