Toronto, Canada (PRWEB) February 28, 2014
Holistic clinical trial insights are improving efficiency in clinical development through timely, integrated data. Armed with critical, actionable insights, medics, clinical project managers, research associates and investigators can identify and take action on potential issues faster than previously possible – but changes are required in how we integrate processes across these roles.
Technology is enabling the evolution of risk-based monitoring by integrating study start-up, clinical monitoring, project management, data management and analytics to optimize and improve clinical trial execution by leveraging risk assessment, ongoing data surveillance, and dynamic monitoring. The results will provide integrated data for holistic trial insights, improved data quality and patient safety, identification and mitigation of risks, and lower costs for more development opportunities.
By attending this webinar, you will:
For more information on this webinar or to register, visit Risk-based Monitoring: Using Centralized Data Surveillance to Evolve Data Review and Site Engagement
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