Simplify and Elevate the Participant Consent Process with iMednet eConsent
iMednet’s Electronic Informed Consent (eConsent) was developed within the iMednet platform to seamlessly integrate, ensuring a secure, simple and efficient electronic consent process for both study participants and site users – and was designed to support the varying needs of traditional, hybrid, and decentralized clinical trials. Participants can review and provide consent at their own pace, anytime, and anywhere. Whether on a smartphone, tablet, or laptop, our responsive design ensures a user-friendly experience across all devices.
Seamlessly track consent status via dashboard
iMednet eConsent ensures compliant collection and storage of electronic signatures along with date/time of consent. Dashboard provides visibility for site users to review the current status of consents and to access completed consents.
Participant-centric, anywhere access
Electronic consent provides an accessible, participant-centric process that saves time and breaks down geographical barriers, enabling researchers to connect with potential participants from around the world.
Highly flexible and configurable
Allows individual participants the choice to complete the eConsent process or to complete a paper consent. Allows the study designer to customize the consent design flow, including multiple page designs to break up the consent into manageable pages. Allows ability to customize wording on the consent form for the Institutional Review Board (IRB) for each site.
Engage and educate with embedded media support
Engage, educate, and enhance participants’ understanding with embedded video or graphics to describe specific study protocol, potential risks and benefits, and the consent process.
User-friendly guidance every step of the way
Intuitive interface guides participants through each section of the consent, ensuring that no critical information is missed.
A custom solution with competitive pricing
iMednet’s custom solution delivers the optimal combination of functionality, flexibility, and affordability.
Ensures a compliant and secure environment
iMednet eConsent employs robust security measures to protect sensitive participant information, maintaining compliance with industry regulations such as HIPAA and GDPR.
Contact us for an introduction to Mednet's comprehensive EDC-centric eClinical platform with key native modules to support all study types and phases – such as randomization, trial supply management, adjudication, ePRO, payments, DICOM imaging, eConsent and more.