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Sara Dyson to Speak at the Medical Device Complaints, MDRS & Reports Workshop

Place

AdvaMed Office in Washington, DC

Start Date

May 23, 2017

End Date

May 24, 2017

Registration Information

Description

How do you implement and measure the effectiveness of a complaint handling system covering a diverse set of possible products and problems? How are complaint files managed across multiple domestic and international facilities? When do complaints rise to the level of MDR's, and how do you handle recalls? What are the current FDA enforcement trends in these areas?  Industry experts and FDA staff will explore these issues during this two day workshop.


This course has been pre-approved by RAPS as eligible for up to 12 credits towards a participant’s RAC recertification upon full completion. 

Inquiries regarding Medmarc should be directed to George Ayd, Assistant Vice President at (800)-356-6886, ext. 309.  Please contact your current broker for additional information regarding what Medmarc can do for you.

Medmarc.  Created in 1979 by the healthcare technology industry, Medmarc's purpose is to be the superior provider of liability insurance and related risk management solutions and to support the development, testing and delivery of products that save lives and improve the quality of life. We offer tailored insurance protection specifically designed for the broad spectrum of needs of the medical technology and life sciences industry. From ideas and prototypes to the reality of commercialization and success - We can Meet Your Changing Needs. www.medmarc.com