Dr. Jeffrey Shuren, director of the FDA's Center for Devices & Radiological Health, details the action plan for implementing changes recommended by an outside consultant.
By Dr. Jeffrey Shuren
FDA’s Center for Devices & Radiological Health (CDRH) is committed to speeding innovative new medical devices to market and to improving the efficiency of our device submission review process. That’s critical for patients getting access to medical devices that treat often life-threatening conditions. It’s also important for industry’s ability to continue developing new products.
Booz Allen Hamilton, Center for Devices and Radiological Health (CDRH), Food & Drug Administration (FDA)
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