jueves, 11 de julio de 2024

Power to the Patient with Patient Generated Health Data By Adrienne R. Lenz, Principal Medical Device Regulation Expert —

https://www.thefdalawblog.com/2024/07/power-to-the-patient-with-patient-generated-health-data/?utm_source=rss&utm_medium=rss&utm_campaign=power-to-the-patient-with-patient-generated-health-data FDA’s Center for Devices and Radiological Health (CDRH) recently partnered with the Digital Medicine Society (DiMe) to host a two-day workshop to help advance the use of patient-generated health data (PGHD) to support improved clinical trials, medical device development, and regulatory science. The workshop included many sessions and panel discussions that focused on how PGHD can be used in patient care and clinical studies to improve health equity. The benefits of PGHD, challenges with PGHD, and future of PGHD were discussed by FDA representatives, industry representatives, patient organizations, and patients.

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