Reducing Regulatory Risk In Clinical Trials With eConsent

Source: CRF Health, a CRF Bracket Company

You may already know too well the challenges of a paper-based Informed Consent process, but did you know that Informed Consent is one of the most cited deficiencies by regulatory authorities? Paper-based informed consent increases your risk for delayed approvals, fines, litigation and even trial failure.

Register for our webinar if you are interested in understanding why these risks occur and how you can leverage electronic informed consent technologies to significantly minimize them.

CRF Health, a CRF Bracket Company