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Best Practices, LLC Report on Post-Marketing Surveillance Programs Sheds Light on Gray Areas of Adverse Event Reporting
Date:4/22/2010

CHAPEL HILL, N.C., April 22 /PRNewswire/ -- The reporting of adverse events continues to be a critical activity for the pharmaceutical industry and its importance is clear as the U.S. Food and Drug Administration increases its focus on post-marketing surveillance for adverse events. Yet when it comes to gray areas like the Internet, reporting practices vary across the pharma industry. A Best Practices, LLC post-marketing surveillance study found that 50 percent of the participating companies don't collect adverse events reports from Internet sources such as blogs or interactive Web events.

This 37-page report will help drug safety leaders navigate the gray areas of the regulations regarding the reporting of adverse events. Best Practices for Post-Marketing Surveillance of Adverse Events within the United States delivers not only metrics around drug safety reporting processes and sources, but also staffing, follow-up activities and compliance training. Drug safety leaders from 15 organizations such as Novartis, Novo Nordisk, Takeda, Boehringer Ingelheim, Wyeth and Amgen shared their practices and insights into the evolving state of post-marketing surveillance of adverse events.

Download a complimentary report summary at: http://www3.best-in-class.com/rr995.htm.

Key topics of this report include:


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SOURCE Best Practices, LLC
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