Clinical Trials Day

Pharmacovigiliance

Timely and accurate information is critical when making decisions affecting human life. Sanjeevani offers both traditional and internet-based solutions to expedite the reporting and tracking of adverse events / serious adverse events.

Services Include
Development of safety databases
Coordination with regulatory and clinical stakeholders
Medical review and coding of Adverse Drug Reaction Reports
Risk signal detection and evaluation
Action Plan development for safety risks
Narrative writing
Regulatory reporting and submissions – CIOMS, MEDWATCH, PSURs, expedited reporting