NRP Event: Sponsor-Investigator Responsibilities

Jamie Kauwell, MHA, CCRC, CHRC
Marisa Corbett, BA, CCRC

Registration for this event is required

Remote attendance is available. Please mute the line and do NOT place on HOLD.
Webex Link
Dial In Number: 1-240-454-0879
Participant pass code: 735 435 161

Learning Objectives:
- Identify sponsor-investigator responsibilities related to clinical research regulations
- Summarize common problems found during FDA inspections
- Apply methods to ensure compliance with regulations and guidelines for sponsor-investigators

Attendance at this event is pending approval for 1 contact hour of clinical research education on applications for Maintenance of ACRP’s CCRC®, CCRA®, CCTI® or CPI® certification designations

Our Mission:
The UNC-NRP is a peer group that is open to all research personnel on campus to promote excellence in the conduct of clinical, social, and translational research through education, professional development and mentoring.


Location information

Brinkhous-Bullitt, room 219

United States
North Carolina
27599 Chapel Hill
North Medical Drive 160

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