Toronto, Canada (PRWEB) November 06, 2013
Much has been discussed around risk-based monitoring, changing the monitoring aspects during clinical development trials, highlighting the impact on roles, patient safety, data quality and cost. But where is this leading Biopharma and medical device development? What might clinical product development look like in 3 years? 5 years?
Dan White has been leading risk-based deployments for over 12 years and will share his views on the next-generation of changes to the evolution of product development. These views include how to identify risks from the protocol design and mitigate risk through execution, and how new technologies facilitate real-time data review by seamlessly integrating data, systems and processes, and therapeutic expertise. With new data integration, how triggers and alerts initiate the right action at the right time for safe, efficient, and high quality trial management, enabling users to drill down into data to gather insights, recognize current and emerging trends, and, make faster, more informed decisions that impact study quality, efficiency and productivity.
From this webinar, you will hear:
Register now to have an open dialog with an industry expert on the changes occurring now, and what the future looks like, for clinical product development. Learn the answers to questions like:
A Q&A with the audience will follow the main presentation.
For more information about this event or to register, visit: http://xtalks.com/next-generation-of-risk-based-monitoring.ashx.
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Michelle Tran, Marketing Manager
+1 (416) 977-6555 ext 284