image goes here
Investigation of Potential Fraud and Misconduct at Clinical Research Sites
When a clinical research organization suspected fraudulent activity potentially impacting data integrity and subject safety across multiple studies and sites, they engaged Advarra Consulting to help them identify the misconduct, implement corrective action plans, and manage regulatory risk.
Advarra Consulting’s regulatory, clinical, and GxP services measurably improved research quality, maintain compliance and delivered on-time study milestones to this organization.
Download the case study to learn more.
Who Should Watch?
Certificate of Attendance
Time: 1 p.m. ET, 12 p.m. CT, 10 a.m. PT
Duration: 1 hour