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When it comes to risk assessment, it’s critical to look beyond what a CRA does.
Over the next few weeks, we will explore how to get started on a risk-based monitoring (RBM) approach in response to ICH E6 guidelines.
Fewer data points will come from the traditional investigator-led EDC data entry process, so what comes next?
In a golden age of mobile applications, how do you develop the apps you need to most efficiently capture and report clinical research outcomes data?
Each month at Medidata we're focusing on a different part of the clinical study process.