Barnes & Thornburg LLP and Pearl IRB invite you to join us for a special event focused on the regulatory aspects of clinical research.
FEATURED PRESENTATIONS:
“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 d‘oeuvres 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: http://www.btlaw.com/Event.asp?Event_ID=918