Clayton Henson

Clayton Henson

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House Passes Bill Relaxing Reporting Requirements

The U.S. House of Representatives recently passed the FDA Reauthorization Act of 2017. This bill seeks to change the requirement for companies to report medical device malfunctions to the FDA. Previously, companies had to...more

8/17/2017  /  FDA Reauthorization Act , Food and Drug Administration (FDA) , Medical Devices , Product Defects , Proposed Legislation , Reporting Requirements
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