Barnes & Thornburg LLP and Pearl IRB invite you to join us for a special event focused on the regulatory aspects of clinical research.


“Responsibilities of the Site and Clinical Research Principal Investigator:  myths and the reality,” Jessica Yaron, RN, MS, Clinical Analyst, inVentiv and Lecturer for IUPUI Research Coordinator Education Program

“What does the new ISO document on GCPs mean for devices?” Gretchen Miller Bowker, COO, Pearl IRB

Moderator: Todd Vare, Partner, Barnes & Thornburg LLP

Location: Event held at the Indianapolis Barnes & Thornburg LLP Law Offices, 11 S. Meridian Street, 5th Floor

AGENDA:  MARCH 15, 2011

Registration            4:00 – 4:30 pm

Presentation/Q&A    4:30 – 5:30 pm

Networking             5:30 – 6:30

Drinks and light hors doeuvres will be served.

Cost: $10

Who should attend: Anyone involved or interested in clinical research, IRB administrators or Board members, research site personnel, sponsors, CROs

Register here: