1. Resource Center
  2. Book Chapter

Risk-Based Monitoring and Fraud Detection in Clinical Trials Using JMP® and SAS®

Chapter 4: Detecting Fraud at the Clinical Site


Is your company moving toward risk-based monitoring of clinical trials as recommended by the FDA? Are you concerned about the integrity and quality of your clinical trials data? Can you tell the difference between bad data and fraud? Richard Zink’s new book Risk-Based Monitoring and Fraud Detection in Clinical Trials Using JMP® and SAS® presents a practical approach for centralized monitoring of clinical trials using JMP Clinical software.

In chapter 4, "Detecting Fraud at the Clinical Site," Zink presents specific examples and explores graphical and statistical approaches for identifying both site- and patient-perpetrated fraud.

Ultimately, says Zink, “A proactive, risk-based approach to quality in clinical trials will more effectively protect the individuals participating in clinical trials.”

*
*
*
*
  Please subscribe me to JMP Newswire, the monthly newsletter for JMP users.
  Yes, you may send me emails occasionally about JMP products and services. I understand that I can withdraw my consent at any time by clicking the opt-out link in the emails.

JMP Statistical Discovery LLC. Your information will be handled in accordance with our Privacy Statement.