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Processing and Handling eMDRs
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What do device manufacturers need to understand about meeting their medical device reporting obligations? Hosted by MD&DI, this FREE Webcast, "Processing and Handling eMDRs," features a panel of industry experts who will share their thoughts on that question. Experts from FDA, an enterprise quality management software provider, and a global medical technology company identify common eMDR pitfalls. The experts also explain how to navigate eMDR regulation and develop an effective reporting system.
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Web event:
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"Processing and Handling eMDRs" |
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Thursday, October 2 |
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3:00 p.m. EDT
2:00 p.m. CDT
12:00 noon PDT |
| Duration: |
50 minutes |
| Who should attend: |
Quality and regulatory personnel from medical device companies. |
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Sponsored by
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"Processing and Handling eMDRs" will feature live presentations by industry experts who have extensive experience in the fields of software, device reporting, and device regulatory practices. Panelists for the Webcast include:
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The Current State of eMDR
Indira Konduri
Chief, Information Analysis Branch
Office of Surveillance and Biometrics, CDRH, FDA
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Implementing an Effective Reporting System
Caren Usrey
Project Coordinator
Allergan Inc.
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Planning and Preparing for eMDR
Don Dougherty
Consultant, Systems Analyst
Allergan Inc.
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Features and Functions of TrackWise eMDR
Peter Hyman
Product Manager
Sparta Systems
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The Webcast will conclude with a
live panel discussion moderated by
Sherrie Conroy,
editor-in-chief of MD&DI magazine.
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TO REGISTER FOR THIS EVENT CLICK HERE
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| ©2008 Canon Communications LLC
The MD&DI Webcast Series is produced by the editors of MD&DI. For more information, please click here.
Canon Communications LLC
11444 W. Olympic Blvd.
Los Angeles, CA 90064
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