The course discusses the fundamental principles and practices involved in document creation, review, approval, and control. In addition, the course explains the function of protocol amendments and their impact on document control.
Language Availability: English
Suggested Audiences: Clinical Research Associates (CRAs), Clinical Research Coordinators (CRCs), Clinical Research Pharmacists, Contract Research Organizations (CROs), Faculty, Investigators, Regulatory Affairs Professionals, Research Administrators, Students, Study Sites
Organizational Subscription Price: Included with the Summit: Document Control and Study Documents 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
