This module is designed to provide clinical trial investigators and research professionals with a comprehensive understanding of the regulatory framework governing medical device trials in Canada. It covers essential topics such as medical device classifications, ISO standards and investigator responsibilities. Practical case studies will help translate regulatory knowledge into real-world applications, offering you the opportunity to engage with authentic trial scenarios. You will learn how to ensure compliance with Canadian and institutional guidelines governing the conduct of clinical trials, navigate the regulatory landscape and manage device-specific responsibilities.​ This module will take about 90 minutes to complete.