Dana Nohynek, Director of Regulatory Affairs and Quality Assurance, provides an overview of how and why to manage risk in clinical trials.

Project Manager Laura Zunino provides an overview of the informed consent process, why it matters, and how to improve it.

Communications and Knowledge Translation Officer Sean Sinden provides an overview of how to integrate sex and gender into research and why it’s important to so.

Evaluation Specialist Glenyth Caragata provides an overview of evaluation studies and how they differ from clinical research.

Senior Project Manager Leslie Love brief overview of regulatory inspections and how to prepare for them.

TAVR Research Manager Dr. Shirley Wong shares what you need to know about conducting trials with medical devices.

Erin Cherban, CHÉOS’ Chief Clinical Research Officer, provides an overview of the changes to GCP guidelines recently adopted by Health Canada.