Leveraging the New eMDR: How to get ahead with electronic medical device reporting

This event is now over, but you can request to view the recorded Webinar. Please fill out the form below. According to the FDA's CDRH, eMDR submissions doubled in 2008, and is expected to at least triple in 2009... In this complimentary Webinar, we examine the FDA's $2.5 billion IT modernization commitment and the reasons why eMDR will most likely be mandated this year. Guidance documents are expected to be published first half of this year. By viewing this Webinar, you'll learn more about the future of eMDR, the options available to you now, and why it makes good business sense to implement an electronic medical device reporting system today. You'll learn more about the FDA's new centralized FAERS (FDA Adverse Event Reporting System) and how it will replace center-centric systems.

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