Supporting Drug Safety with PharmaPendium and advanced FAERS searching
Presented by
Sherry Winter
About this talk
Drug safety considerations impact the entire drug development lifecycle, from preclinical safety assessments to clinical trials to post-market.
In this webinar, we will discuss how to leverage the comparative FDA and EMA regulatory information in PharmaPendium to inform translational and clinical development decisions, as well as to strengthen regulatory approval strategies.
Realize the potential of data-driven drug discovery and development with solutions that help you increase research efficiency and ensure a thriving R&D pipeline.…