Fraud in Clincal Research May 2010

May 12, 2010


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Fraudulent activities in clinical research undermine clinical research professionals’ ability to meet their obligations for ensuring credible data is obtained from protected participants. This course provides an overview of fraud in clinical research and its potential impact on the industry and the public’s health.

Discuss significant and current examples of fraud in clinical research
Describe the current focus of regulatory and Congressional bodies
Explain the Sponsor/CRO, IRB, Clinical Investigator, and Study Staff role in detection and prevention
Recognize the impact and consequences of fraud in clinical research
Landmark and recent cases of fraud in clinical research
Regulatory authorities’ current focus and findings
Group discussions of best practices

Clinical Quality Assurance Professionals
Clinical Research Associates
Project Managers
Clinical Investigators
Study Coordinators
IRB Professionals
Institutional Officials involved in oversight of clinical research
Data Management Professionals
Regulatory Affairs Professionals

Elizabeth Ronk Nelson, MPH

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2 hours 1:00 - 3:00 p.m. Eastern

May 12, 2010

Hold this course at your company!

For more information, contact Naila Ganatra at (215) 413-2471

On-Demand GCP Refresher Training

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Barnett "Hands-On" Workshops are designed to provide intensive, hands-on training in a highly targeted clinical research topic area in a very interactive and engaging learning environment. To view more details and available courses, click here.

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