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Description
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.
Audience
Clinical Research Associates (CRAs), Clinical Research Coordinators (CRCs), Contract Research Organizations (CROs), Faculty, Investigators, Research Administrators, Sponsors, Students
Meet the Presenter
I am a medical professional with 20+ years of pre-hospital emergency medical service experience, an honorably discharged veteran with 5 years of service in the US Navy (Reserve), and a dedicated, goal-oriented, quality-driven instructor and mentor with nearly 20 years of global pharmacovigilance experience.
