eConsent w/Private Access

PrivateAccess™ allows systems the ability to provide patients clear and easy-to-understand clinical trial information so that they are truly informed to make a decision to participate in research trials or studies.  It also offers sites
tools to get insight into the patient’s understanding and reduce complex & time-consuming explanations, paperwork and quality risks.

PrivateAccess™ also helps establish a consistent and aligned process for Health Authorities and Ethics Committees to improve review/approval process & reduce inspection findings, and reduces or eliminates on-site consent monitoring activities and corrective actions for audit/inspection consent findings for sponsors; improve patient recruitment and reduce dropout rates for complex studies.

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