Drug safety and pharmacovigilance are key in developing drugs, biologics, and medical devices. This webinar defines drug safety concepts and terms while detailing the types and sources of safety information. It describes the life cycle of handling individual case safety reports (ICSRs) and explores the interactions of drug safety and pharmacovigilance with other functional areas of biomedical product research.
Release Date: February 26, 2025
Language Availability: English
Suggested Audiences: Clinical Research Associates (CRAs), Clinical Research Coordinators (CRCs), Contract Research Organizations (CROs), Faculty, Investigators, Research Administrators, Sponsors, Students
Organizational Subscription Price: Included as part of an annual subscription to our All Access Webinar Package
Independent Learner Price: $49 per person
