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    Handling Adverse Events in a Changing Postmarket World

In response to widespread public concern about the safety of approved medical devices, FDA is moving rapidly to reinvigorate its mechanisms for postmarket monitoring. This FREE Webcast, “Handling Adverse Events in a Changing Postmarket World,” will examine the new policy environment for medical products and what it will mean for medical device companies. Hosted by MX magazine and sponsored by Oracle Corp. and Deloitte Consulting LLP, the Webcast will explain how advanced CAPA and complaint-handling systems can help manufacturers meet FDA's emerging requirements for more-stringent postmarket surveillance.
Web Event: Handling Adverse Events in a Changing Postmarket World
Date: Thursday, February 22
Time: 2:00 p.m. EST
1:00 p.m. CST
11:00 a.m. PST
Duration: 50 minutes
Who should attend: Senior management involved in regulatory compliance and quality systems development.
   TO REGISTER CLICK HERE
"Handling Adverse Events in a Changing Postmarket World" will feature three live presentations by industry experts with extensive experience in the field of regulatory compliance systems and postmarket monitoring. Panelists for the Webcast include:

Transforming the Future: FDA's Changing
Postmarket Policy
Michael M. Breggar
Director, Life Sciences and Health Care
Deloitte Consulting LLP

Closing the CAPA Loop: The Role of
Advanced Information Technologies
Dennis Constantinou
Senior Director, Life Sciences Strategy and Marketing
Oracle Corp.

Leading Practices in Medtech Complaint Management
Raj Jayashankar
Senior Manager
Life Sciences and Health Care
Deloitte Consulting LLP


The Webcast will conclude with a
live Q&A session moderated by
Steve Halasey
Editor in Chief of MX magazine.

TO REGISTER FOR THIS EVENT CLICK HERE

Sponsored By:

 

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