Embedding AI and Critical IRB Operations Data to Drive Intelligent Study Design

Study design is increasingly empowered by a rich and diverse array of data. New sources continue to emerge, fueled by advances in AI that enable the integration of information from literature, ClinicalTrials.gov, digitized protocols, and beyond. Harnessing these complementary data streams allows researchers to design studies that are not only operationally efficient but also more inclusive, informed, and scientifically sound.

In this webinar, IDC analyst Dr. Nimita Limaye, Research VP, Life Sciences R&D, Strategy and Technology, joins Advarra’s Managing Director Ian Bailey for a dynamic discussion on how the industry can critically evaluate and integrate these data streams into their study design decisions. They will also investigate critical use cases, analytical models, and AI techniques that can transform these inputs into meaningful insights to optimize study design and maximize operational potential for pharma leaders.