Event:
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Detecting and Preventing Fraud in Clinical Research
- Hosted By:
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ComplianceOnline
- Start:
- Monday - Sep 16, 2013 10:00 AM
- End Time:
- Monday - Sep 16, 2013 11:00 AM
- Location:
- Online
- This webinar will discuss methods for detecting and reporting falsified or fabricated clinical data and present techniques for preventing fraud in clinical research.
Why Should You Attend:
The consequences of clinical research fraud are severe and far reaching because it may take a long time to uncover fraud and this can result in severe consequences for drug companies who have submitted data which is later determined to be fraudulent. Regulatory authorities are getting better about fraud detection.
This session will critically examine fraud in clinical research and show how clinical trial staff can effectively detect and prevent fraud. The presenter will discuss case studies of recent high profile frauds to help participants understand who commits fraudulent acts and how fraud is presented in clinical trials. You will learn how regulatory agencies and the clinical research industry are responding to detect and contain fraud.
This session will explore methods for detecting and reporting falsified or fabricated clinical data and present techniques for preventing fraud.
Areas Covered in the Webinar:
Fraud and misconduct defined
What motivates fraud in clinical research - why and how fraud occurs
Regulatory background and focus
High profile case studies of fraud in clinical research
Conflict of interest (CoI)
Practical methods to detect Fraud
Proven techniques to prevent fraud
Who will benefit:
This webinar will provide valuable assistance to:
Experienced clinical trial staff members
Healthcare providers interested in exploring the field of Clinical Research
New Clinical Research Coordinators (1-2 years)
New Principal Investigators
Administrative managers in charge of Clinical Research
Regulatory Compliance Associates and Managers
- Website:
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Visit the website for detail info