Pragmatic Clinical Trials (PCTs) challenge traditional research ethics by intentionally integrating research and clinical care, prompting unique ethical and regulatory considerations. This webinar explores the distinct ethical paradigm governing PCTs compared to conventional clinical research, rooted in foundational principles like those outlined in the Belmont Report and Common Rule. The webinar also examines key issues including informed consent, data and safety monitoring, and data sharing, as well as institutional factors impacting PCT implementation. The webinar is designed for clinical and regulatory professionals seeking to balance ethical standards with the practicalities of achieving meaningful, real-world outcomes through clinical research.
Webinar Demo:
Release Date: August 19, 2025
Language Availability: English
Suggested Audiences: Compliance Professionals, Faculty, IBC Administrators, Postdocs, Research Administrators, Students
Organizational Subscription Price: Included as part of an annual subscription to our All Access Webinar Package
Independent Learner Price: $49 per person
