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| Clinical research and development is using risk-based monitoring (RBM) to improve patient safety and study quality, while reducing costs for trials in all therapeutic areas and in all phases |
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| Attend this live webinar to learn of results from over 200 executed RBM studies, and understand the benefits of the latest technology advancements for Centralized Monitoring to automate your business processes, provide insights into potential safety & performance issues, and deliver more informed, faster insights for your clinical trials. |
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| Key take-aways: |
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| Execute your RBM trials with confidence as the next wave of Centralized Monitoring provides: |
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Enhanced patient safety throughout your trials, regardless of therapeutic area or trial phase |
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Improved site and overall study efficiencies with automated, auditable workflows for faster, centralized issue management |
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Faster identification and mitigation of risks, while automating plans using a Quality by Design approach to your trials |
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| Presenters: |
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Zabir Macci
Process Design & Analytics Manager, QuintilesIMS
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Rajneesh Patil
Senior Director, RBM and Analytics, QuintilesIMS |
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| Moderator: |
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Lisa Henderson
Editorial Director, Applied Clinical Trials |
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For technical questions about this webinar,
please contact Kristen Moore at kristen.moore@ubm.com |
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Contact us at
www.QuintilesIMS.com
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