The focus of this webinar is “Navigating FDA Regulations for Canadian Clinical Trials”. The speaker Eric S. Pittman from Office of Regulatory Affairs’ (ORA), FDA, will discuss FDA regulatory frameworks, differences from the Canadian regulations, and how to navigate compliance and manage regulatory audits. This is an excellent opportunity for everyone involved in clinical research to stay informed about crucial regulatory requirements. I encourage everyone to register for this FREE webinar.
Webinar Information:
Topic: Navigating FDA Regulations for Canadian Clinical Trials
Presenter: Eric S. Pittman, Program Division Director, Bioresearch Monitoring West (BIMO-W), Office of Regulatory Affairs’ (ORA), Office of Bioresearch Monitoring Operations, Food and Drug Administration (FDA)
Date: Wednesday, July 17th, 2024
Time: 11:00 AM -12:30 PM EST
Registration Link: https://hhsc.zoom.us/webinar/register/WN_Di3ZQoitR2qEi3vnMhLlew
Pleae find flyer here: Webinar.pdf
