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FDA Releases Plan For Enhancing eMDR Adverse Event Reporting System

 
• By Shawn M. Schmitt

The US agency has announced some changes it plans to make to its electronic Medical Device Reporting system over the coming year.

FDA building.
• Source: Shutterstock

The US Food and Drug Administration on 8 July released its annual list of changes the agency plans to make to its electronic Medical Device Reporting (eMDR) system.

The agency says its enhancements over the next 12

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