Adverse Events Reporting

The Penn Human Subjects Adverse Events Reporting System (PennAEs) is a web-based system that gives principal investigators (PIs), clinical coordinators, and staff in the Office of Regulatory Affairs a means of tracking, collecting, and reporting serious adverse events in clinical trials involving human subjects to the Institutional Review Boards of the University of Pennsylvania. For more information about the PennAEs system, visit the Office of Regulatory Affairs web site at http://www.upenn.edu/regulatoryaffairs/human/AdverseEvents.html or send an e-mail to pennaes@pobox.upenn.edu.