eClinical

eConsent incorporates a powerful suite of multimedia tools to optimize the participant informed consent experience. By offering a range of components suited to different learning styles, eConsent offers site managers the flexibility to fully engage participants, obtain quality data, and automate information collection for maximum reliability.

Advarra eReg improves regulatory staff productivity, boosts compliance, and reduces the cost of regulatory management at your organization. A comprehensive system developed in close collaboration with leading academic medical centers, cancer centers, and health systems, eReg streamlines regulatory management and provides turnkey integrations with your enterprise systems.

Processing paper forms can create numerous obstacles for your clinical trial site, including added labor hours, patient confusion, and a risk of errors. Advarra eSource allows you to gather data digitally, increasing your site’s cost efficiency, improving the participant experience, reducing study delays, and elevating the quality of the information your staff collects.