Article | June 7, 2018

Monitoring Clinical Trials With Electronic Informed Consent

Source: CRF Health, a CRF Bracket Company

By Sandra “SAM” Sather, VP, Clinical Pathways, Regulatory & Quality, TrialConsent – CRF Health & Neetu Pundir, Market Director - CRF Health

This article highlights some of the monitoring challenges and burdens related to informed consent for a clinical trial and explains how electronic informed consent (eConsent) can positively impact monitoring practices and documentation. The article demonstrates how oversight of data integrity and human subject protection may be improved with an eConsent solution and provides some guidance on considerations when implementing eConsent in a clinical trial to enhance the monitoring process, including saving time, reducing costs and boosting efficiencies.

CRF Health, a CRF Bracket Company