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Adverse Event Reporting in Clinical Trials: How to Minimize Your Liability by Working With Investigators

Written by on Monday, December 4th, 2006 Print This Post Print This Post

The teleconference  Adverse Event Reporting in Clinical Trials: How to Minimize Your Liability by Working With Investigators will take place on December 14, 2006 from 1:00 – 2:30 p.m. EST. The cost is $299 per listening site, and the persenter will be Stephen Schwartz, director of clinical services for Solaris Research Corporation.  This presentation will cover the following issues:

  • How to avoid underreporting—and equally dangerous overreporting;
  • The role of evaluating study patient AEs; and
  • Which specific events are considered “adverse” and which should be reported. 

To register, call toll-free at 800-688-2421.

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