NIH Clinical Trials Requirements, FORMS-E, and the Common Rule: What You Need to Know

November 14, 2017 - 12:00pm to 1:00pm

Jean Barone, CIP - Director, HRPO
Kelly Dornin-Koss, MPPM, RN, CIP, CCRC - Co-Director, RCCO; Director, ECO
Laura Kingsley, MPH, CRA - Senior Associate Director, Office of Research
Shannon Valenti, MBA - Research Facilitator, CTSI

There are many changing regulatory and policy requirements for researchers and administrators to manage.  Join representatives from the Human Research Protection Office, Research Conduct and Compliance Office, Office of Research, and Clinical and Translational Science Institute to learn about new requirements, brush up on long-standing requirements and learn how these University offices interact with one another. Topics to be discussed include the new Common Rule, NIH clinical trial definition and requirements, NIH FORMS-E expanded questions, CTSI resources and GCP training requirements.

No pre-registration is required and all are welcome to attend. Email Melissa at with any questions. Click here to view the presentation.


Directions and Parking Information

Biomedical Science Tower South, Room S120
220 Darragh Street
Pittsburgh, PA 15213