Falsifying Data in clinical trials. What to report?
Why Should You Attend: Falsifying data in clinical trials can be devastating to the researcher and the institution. Not all activity that is questionable involves a violation of research integrity so knowing who to ask or where to go for guidance can help avoid a compromising situation. During this 60-minute session, participants will get a clear understanding of what type of activities should be reported, by who and when. It will use case studies to explain instances of falsification, fabrication and plagiarism. The presenter will also discuss regulations governing the ethical conduct of human subjects research. The objective of this course is to help participants understand the rules, before and while the research is conducted, so they can create a culture of compliance which helps avert problems. Areas Covered in the Webinar: -What is research integrity? -Definitions for falsification, fabrication and plagiarism -What types of problems are created? -What should be reported? -Where should those reports go? -Who monitors and governs research integrity? Who Will Benefit: -This webinar will provide valuable assistance to all personnel in: -Human Subjects Research -Clinical Research Coordinator positions -Investigator positions -Administration in charge of Clinical Research -Regulatory Compliance For Registration: http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=703134?channel=limsfinder
