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Setting The Standard In Personal Injury Law

May 2011 Archives

High-Risk Devices Being Fast-Tracked?

Medical professionals rely upon medical devices every day when treating patients with serious injuries or illnesses. Both patients and doctors alike rely upon the devices being used, and trust that they are going to be able to solve whatever problems may be occurring. Before devices can be used, they must be approved by the Food and Drug Administration (FDA). The approval process is falling under heavy scrutiny after several high-profile issues have raised concerns over the agency's fast-track approval process.

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