Investigator Selection & Site Monitoring

The life science industry is fully aware of the guidance around site monitoring and it is widely known
and accepted to be one of the most costly and resource-intensive functions of any clinical trial.
Currently it is estimated almost one third of the cost of a clinical trial is spent on monitoring activities.
To date, most sponsors and contract research organizations (CROs) have primarily invested in
electronic data capture (EDC) as a technology that offers the promise of reducing the time to
submission from database lock therefore enabling them to expedite the submission process and gain
faster approval.


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