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The U.S. Food and Drug Administration’s (FDA) Center for Devices and Radiological Health (CDRH) is accepting site proposals for the Spring 2024 cycle of the Experiential Learning Program (ELP). Through this collaborative learning experience, sites host CDRH staff (virtually or in-person) and share with them valuable insights about medical devices, emerging technologies, industry practices, regulatory processes, and patient needs.
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About the program: Through one- or multi-day (virtual or on-site) visits, CDRH staff gain real-world knowledge of new and existing medical devices and radiation-emitting technologies, laboratory practices, industry policies, quality systems management, and how patient needs affect medical device development.
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Who participates: CDRH welcomes site proposals from medical device manufacturers, academia, clinical facilities, medical device incubators and accelerators, health insurers, health technology assessment groups, and other medical device stakeholders, including those that have previously participated in the ELP or other FDA programs.
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How to participate: Submit site proposals for ELP’s Spring 2024 cycle before Friday, March 8, 2024, at noon EST.
Sites can select which topics to highlight during the visits, and proposals can be related to any of the areas of interest that are listed online.
Questions?
If you have questions about ELP’s Spring 2024 cycle, please contact the ELP Program Manager at ELP@FDA.HHS.GOV.
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