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The Impact of RBM on Site Monitors

Everything Clinical Trials

Kalyani Nayaka - October 13, 2017

The Impact of RBM on Site Monitors

Sign up to attend Medidata’s GLOBAL NEXT event in New York City from November 8th through the 10th and claim your seat today.
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Common Misconceptions About Centralized Monitoring

Everything Clinical Trials

Kalyani Nayaka - October 4, 2017

Common Misconceptions About Centralized Monitoring

For starters, centralized monitoring is not a one-person function.
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The Case for Centralized Monitoring

Everything Clinical Trials

Kalyani Nayaka - September 27, 2017

The Case for Centralized Monitoring

With the rise of risk-based monitoring, we must move away from a 100% SDV approach.

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Starting a Risk Assessment? Start Early

Everything Clinical Trials

Kalyani Nayaka - September 20, 2017

Starting a Risk Assessment? Start Early

When it comes to risk assessment, it’s critical to look beyond what a CRA does.
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Cross-functional Perspectives Are Crucial For Risk Assessment

Everything Clinical Trials

Kalyani Nayaka - September 11, 2017

Cross-functional Perspectives Are Crucial For Risk Assessment

Risk assessment must go beyond the concerns of operations or monitoring teams and span the entire organization – because the conversation is no longer just about monitoring.
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