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Audio conference highlights
Inefficient medical device reporting presents a clear and present danger: It can damage your company’s reputation and even threaten your ability to operate. After sending some mixed signals in the second half of 2007, FDA eMDR experts have said they’ll mandate eMDR within two years. The only debate now is how quickly it will happen, and what kind of timeline mandate will be imposed.
It’s therefore not surprising to learn the agency is pushing harder for electronic medical device reporting than anyone else. In this audio conference, 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.
This audio conference covers:
- The choices for electronic medical device reporting today
- How eMDR works
- Why it will eventually be mandated by the FDA
- How MDRs are handled today by the FDA
- Why it's good strategy to get an early start
About the speaker:
Tamar June is the Vice President of Strategic Marketing and Product Manager for eMDR for AssurX, Inc. She has been in the information technology and manufacturing industry for more than 15 years and has published numerous FDA-related and medical device regulatory and technology articles appearing in a variety of publications.
She holds a B.S. degree in marketing from St. Joseph’s University and attended the Katz Graduate School of Business at the University of
Pittsburgh.
Who should attend?
- VP - Quality, Regulatory
- Product Surveillance
- Post-market Surveillance
- Quality Managers
- Regulatory Managers
*Please note: Each registration covers one line connected to the audio conference. Attendees dialing from separate locations are required to have separate registrations.