Tessa is a specialist in literature monitoring solutions for pharmacovigilance. I advise on all aspects, from optimizing search strategies for precision and recall to streamlining the literature review process using validated software. I work with all sizes of pharmaceutical organisations and focus on introducing automation, providing ROI, increasing oversight, tracking KPIs, reducing workloads, reducing risk and increasing inspection readiness
With the rapid adoption of AI, driving patient safety with pharmacovigilance in a compliant manner is more attainable than ever, reducing workload and maintaining oversight.
In this session, we’ll explore strategies to manage the ever-growing volume of safety information and how AI can reduce costs and save valuable time for pharmacovigilance teams. Explore how AI research assistants can help with ad-hoc queries for aggregate reporting and the assessment of potential signals within the context of class safety intelligence.