FDA/Patient Workshop

The Food and Drug Administration’s (FDA) Center for Devices and Radiological Health (CDRH) is announcing an interactive, in-person workshop entitled “Partnering with Patients on CDRH’s Research Agenda for Assistive and/or Neurostimulation Devices”

The purpose of this workshop is to receive feedback on patient needs and experience regarding the usability, benefits, and desired features of medical devices to inform the regulatory science research agenda at the CDRH.  This workshop will focus on Assistive and Neurostimulation devices associated with subpopulations of the following diseases as examples:

  • Diabetes
  • Lupus
  • Macular Degeneration
  • Neurological Diseases

The interactive sessions will involve patients who wear these devices; providers, caregivers, clinicians, and medical personnel who work with these patients.

  • Date, Time and Location
  • Registration
  • Agenda
  • Contact Us

FDA Campus Information

[email protected].

For questions regarding workshop content please contact:

Marilyn M. Lightfoote, Food and Drug Administration, Center for Devices and Radiological Health, 10903 New Hampshire Avenue, Silver Spring, MD 20993, email: [email protected].