MedWatch Plus: Preparing for Electronic Adverse Events Reporting in the US
This article was originally published in RAJ Devices
Executive Summary
The Food and Drug Administration is pressing on with plans to make electronic reporting of adverse events mandatory. Brenda Percy examines how companies can make a seamless transition from paper to electronic submissions.
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MedWatch Plus: Preparing for Electronic Adverse Events Reporting in the US
The Food and Drug Administration is pressing on with plans to make electronic reporting of adverse events mandatory. Brenda Percy examines how companies can make a seamless transition from paper to electronic submissions.