U.S. Food and Drug Administration | Module 5 – Why Use Models to Inform Decisions? @US_FDA | Uploaded 2 months ago | Updated 4 hours ago
Dr. Mark R. Gasronguay, Founder and CEO of the Metrum Research Group, asks “why use models?” when there’s observed data, and discusses how models can be used to derive insights around unstudied conditions.
This module is part of the educational series “Model-Informed Drug Development (MIDD): Methods Advancing Medical Products to Patients”. The educational content was developed for regulatory scientists by experts in the field in partnership with the Critical Path Institute and funded by FDA CDER Office of Translational Sciences. As part of Multidisciplinary Education and Exchange initiatives, CDER’s Quantitative Medicine Center of Excellence is making this resource accessible to all, supporting community-wide educational enrichment.
Disclaimer: The presentations in this educational series reflect the views of the presenters and should not be construed to represent FDA’s views or policies.
Dr. Mark R. Gasronguay, Founder and CEO of the Metrum Research Group, asks “why use models?” when there’s observed data, and discusses how models can be used to derive insights around unstudied conditions.
This module is part of the educational series “Model-Informed Drug Development (MIDD): Methods Advancing Medical Products to Patients”. The educational content was developed for regulatory scientists by experts in the field in partnership with the Critical Path Institute and funded by FDA CDER Office of Translational Sciences. As part of Multidisciplinary Education and Exchange initiatives, CDER’s Quantitative Medicine Center of Excellence is making this resource accessible to all, supporting community-wide educational enrichment.
Disclaimer: The presentations in this educational series reflect the views of the presenters and should not be construed to represent FDA’s views or policies.
