Adverse Event Reporting in Clinical Trials: How to Minimize Your Liability by Working With Investigators
Written by Kristie Prinz on Monday, December 4th, 2006
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.
Category: Biotech Industry Events