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Advancing the Discipline of Regulatory Science for Medical Product Development: An Update on Progress and a Forward-Looking Agenda: A Workshop

Completed

The Food and Drug Administration (FDA) defines regulatory science as the science of developing new tools, standards, and approaches to assess the safety, effectiveness, quality, toxicity, public health impact, or performance of FDA regulated products. This workshop provided a venue to review progress in building the foundations of regulatory science and explore a forward-looking agenda for bolstering the field. Participants examined the current state and scope of the discipline, highlight opportunities to address barriers to success, and explore ways to foster collaboration.

Please visit our event page for additional information and meeting materials for the workshop (held on October 20-21, 2015)

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