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Risked Monitoring (RBM), a mechanism to optimize clinical trial
monitoring process
Life sciences organizations are faced with the Infosys RBM solution attempts to multitude of challenges:improve the
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What is risk-based monitoring rbm a?
RBM is a quality-focused, proactive, and data-driven approach to monitoring clinical trials.
Who is required to file risk-based monitoring rbm a?
Sponsors of clinical trials are required to implement RBM.
How to fill out risk-based monitoring rbm a?
RBM is filled out by analyzing data to identify and prioritize risks during clinical trials.
What is the purpose of risk-based monitoring rbm a?
The purpose of RBM is to enhance patient safety, data quality, and overall study efficiency.
What information must be reported on risk-based monitoring rbm a?
Information related to risk identification, risk mitigation strategies, and monitoring activities must be reported on RBM.
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