F. Regulatory and Clinical Development
Pharmacovigilance and Drug Safety
Provides an overview of post-marketing safety activities, adverse-event reporting, case processing, causality, signal detection, periodic reporting and risk management.
Duration12 hours
Best ForPharmacists, regulatory staff, medical teams and safety personnel
FormatRecorded, live or customized
Provides an overview of post-marketing safety activities, adverse-event reporting, case processing, causality, signal detection, periodic reporting and risk management. It emphasizes organizational responsibilities and timely, complete, high-quality safety information.