||Risk-Based Monitoring: 5 Mistakes To Avoid
Event Date: February 19, 2015 11:00 am ET | 4:00 pm BST
With the expansion of risk-based monitoring (RBM) capabilities comes the need to clearly understand the ramifications on patient safety, data quality and clinical trial costs. This webinar will address some of the top mistakes made during the evaluation of risk-based monitoring technologies and provide forward looking insights into key developments affecting the future of RBM including adaptive monitoring, data surveillance and integrated data management.
This webcast will include:
Who should attend:
Pharmaceutical and biotechnology professionals involved with managing clinical trials.
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