This course introduces the fundamental principles and practices of conducting clinical trials. It examines the functions of study protocols, the requirements for informed consent, and the role of Institutional Review Boards (IRBs). It examines the best practices for maintaining patient safety and data integrity.
Language Availability: English
Suggested Audiences: Clinical Research Coordinators (CRCs), Clinical Research Pharmacists, Contract Research Organizations (CROs), Faculty, Investigators, Regulatory Affairs Professionals, Research Administrators, Study Sites
Organizational Subscription Price: Included with the Summit: Clin Ops Foundations series, available for $675 per year/per site as a subscription add-on for government and non-profit organizations; $750 per year/per site as a subscription add-on for for-profit organizations
Independent Learner Price: $99.39 per person
