Clinical Compliance 2012 - Safety Reporting in Clinical Trials: Are you Compliant with the Current FDA Rules?

This Safety Reporting in Clinical Trials webinar will review FDA's recent major revisions to IND safety reporting requirements. It will explain FDA's current expectations of sponsors, investigators, IRBs, and other personnel responsible for reporting safety related information while conducting clinical trials with a new investigational product or a generic drug.

If your company or organization is involved in clinical trials, if you are a clinical site or safety monitoring/pharmacovigilance organization, if you with an IRB overseeing clinical trials, or if you are not sure of your compliance status with the current regulations, you can get valuable tips and training in less than an hour.