FDA CDRH to Hold Series of Webinars on Electronic Medical Device Reporting

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We recently blogged about electronic medical device report (eMDR) submissions to CDRH setting new records in 2010. Looks like the FDA would like to get more medical device companies on the bandwagon by offering a series of monthly interactive Webinars. An email sent today from Eugene Reilly states:

Many MDR reporters are already submitting MDRs electronically, but many still have not taken the plunge. If you’re one of those, why wait?  Find out all you need to know to take the mystery out of electronic reporting at one of our upcoming interactive webinars and meet CDRH’s eMDR Team:

Friday, April 29, 2011
1:00 PM–5:00 PM EDT (1:00–1:30: Technical webinar issues/questions handled.)

Friday, June 03, 2011
1:00 PM–5:00 PM EDT (1:00–1:30: Technical webinar issues/questions handled.)

Friday, August 05, 2011
1:00 PM–5:00 PM EDT (1:00–1:30: Technical webinar issues/questions handled.)

Friday, September 30, 2011
1:00 PM–5:00 PM EDT (1:00–1:30: Technical webinar issues/questions handled.)

Friday, November 18, 2011
1:00 PM–5:00 PM EDT (1:00–1:30: Technical webinar issues/questions handled.)

CDRH’s Webinar Connection Information:
We encourage participants to test your connection prior to the webinar. Participants will not be able to enter the actual meeting until the host has logged in on the day of the event.

To join the meeting (Please use your email address to join the Adobe Connect session. We will use this email address to send follow-up information.):
https://collaboration.fda.gov/cdrhemdr/

To test your connection: https://collaboration.fda.gov/common/help/en/support/meeting_test.htm

To get a quick overview:
http://www.adobe.com/go/connectpro_overview

Questions? Please feel free to e-mail us at eMDR@fda.hhs.gov

No news yet on a mandate.

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