Clinical Trials Roles and Responsibilities: The Sponsor, The Institution and the Qualified Investigator – Apr. 19, 2023

Session Description

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Clinical Trials Roles and Responsibilities of The Sponsor, The Institution and the Qualified investigator in Clinical Trials, is a vast topic many researchers and teams have expressed interest in learning more about. This is also an area many teams receive observations during regulatory inspections. Health Canada representative, Asma Syed, will be joining the upcoming webinar on April 19th to help us have a better understanding of this important topic. Asma is a Field Operations Supervisor for the Clinical Trials Compliance Program, Regulatory Operations and Enforcement Branch at Health Canada. Questions for Asma can be submitted to RCSS@hhsc.ca in advance of the webinar.

Ms. Asma Syed holds a Masters of Science degree in clinical trials from the University of London. She started her career with the public service in 2001 with the Health Products and Food Branch, where she held various regulatory positions related to biologics, cells, tissues and organs and good clinical practices. She spent 9 years at the Department of National Defense working as a Regulatory and Product Development Specialist. Asma worked with national and international partners to develop and gain approval in Canada for various drug products and medical devices for military use. She joined the Regulatory Operations and Enforcement Branch in 2019 as the Field Operations Supervisor for the Clinical Trials Compliance Program.

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