FDA looks at home-based medical devices

The U.S. Food and Drug Administration on Tuesday said it was going to begin monitoring the use of medical devices in home settings.
The federal agency is currently developing a guidance document for devices used to treat kidney failure, wound therapy care, intravenous therapy and ventilators. This summer, it is asking manufacturers of these devices to voluntarily submit their labeling to the agency.
To learn more about the regulatory changes, visit www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm209138.htm

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