March 14, 2019
Nora Schmitt will be participating in a webinar entitled “Clinical Trials and Human Research Compliance: New FDA Guidance and Revised Common Rule: Complying with Agency Regulations for Informed Consent, Expedited Review, and IRB Continuing Review” on Thursday, March 14th from 1:00 pm - 2:30 pm.
This CLE webinar will guide counsel for navigating agency regulations and the Common Rule revisions for clinical trials and human subjects research. The panel will discuss the new Food and Drug Administration (FDA) guidance, examine the practical impact for stakeholders such as hospitals, research organizations and drug manufacturers, and will outline compliance strategies to meet the regulatory requirements. Click here for more information.