New in CCRM: List of Tracked Devices

June 6, 2014 | Aging Services Risk, Quality, & Safety Guidance

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The U.S. Food and Drug Administration (FDA) requires manufacturers, hospitals, nursing homes, home health agencies, and other organizations that distribute medical devices to collect information about certain medical devices used in patient and resident care so that the device can be promptly identified and recalled if it presents a serious risk to an individual's health.

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