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Technology is continuously evolving and the FDA’s Center for Devices and Radiological Health (CDRH) Experiential Learning Program (ELP) provides CDRH review staff with an opportunity to visit sites and gain a better understanding of the products they review. The 2023 ELP Site Visit Proposal period is open now until September 6, 2022 at 12pm EST. CDRH encourages participation from medical device manufacturers, academia, and clinical facilities, medical device incubators and accelerators, health insurers, health technology assessment groups, and others, including those that have previously participated in the ELP or other FDA site visit programs.
The ELP Program:
- Provides CDRH review staff with opportunities to better understand current industry policies, innovative technologies, laboratory practices, how patient input affects medical device development, and quality systems management.
- Is a collaborative effort to close the knowledge gap between emerging and innovative technology and the pre-market review of the resulting medical devices.
Questions?
If you have questions regarding the Experiential Learning Program, please contact the ELP Program Manager at ELP@FDA.HHS.GOV, or (240) 402-2246.
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