Expert discusses benefits of eMDR system to FDA's device center

02/21/2010 |

The electronic medical device reporting system is meant to help the FDA's device center address the rise in report submissions and prevent human error for encoding data, among other benefits, said Debra Kacera, Pilgrim Software's senior product manager of regulatory products, at a webinar hosted by the Advanced Medical Technology Association. Kacera also discussed the steps on how to electronically submit reports to the FDA through the eMDR system as well as the approaches that may be used by device makers in filing electronic reports.

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