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Synopsis
Improve efficiency while reducing costs in clinical trials with centralized monitoring techniques using JMP and SAS.
International guidelines recommend that clinical trial data should be actively reviewed or monitored; the well-being of trial participants and the validity and integrity of the final analysis results are at stake. Traditional interpretation of this guidance for pharmaceutical trials has led to extensive on-site monitoring, including 100% source data verification. On-site review...
About the Author
Richard C. Zink is a Principal Research Statistician Developer in the JMP Life Sciences division at SAS Institute. He is a developer for JMP Clinical, an innovative software package designed to streamline the review of clinical trial data. He joined SAS in 2011 after eight years in the pharmaceutical industry, where he designed and analyzed clinical trials for patients diagnosed with chronic hepatitis B infection, chronic myeloid...
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- PublisherSAS Institute
- Publication date2014
- ISBN 10 1612909914
- ISBN 13 9781612909912
- BindingPaperback
- LanguageEnglish
- Number of pages268
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Risk-Based Monitoring and Fraud Detection in Clinical Trials Using JMP and SAS
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SAS Institute (edition ), 2014
ISBN 10: 1612909914
ISBN 13: 9781612909912
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Risk-Based Monitoring and Fraud Detection in Clinical Trials Using JMP and SAS
Published by
SAS Institute (edition ), 2014
ISBN 10: 1612909914
ISBN 13: 9781612909912
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Risk-Based Monitoring and Fraud Detection in Clinical Trials Using JMP and SAS
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