CDRH pulls data from other regulators for risk assessments

06/22/2008 | FDAnews

The FDA's Center for Devices and Radiological Health will continue working to tap other regulators' data to improve risk evaluations of medical-device production plants, Office of Compliance Director Timothy Ulatowski said. Ulatowski will attend the fifth annual Medical Device Quality Congress this week to discuss the CDRH's priorities.

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