Product Overview
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.
Deployment
- Web based
- Cloud Hosted
Pricing
- Subscription
- License Fee
More Information
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.
About the company
Mednet is a leading healthcare technology company specializing in eClinical solutions designed for the global life sciences community.
With more than two decades of experience and thousands of studies conducted with both CROs and life sciences sponsors, we have the knowledge and experience to help you achieve success. From our Leadership to our Board of Directors to our product development experts and professional services teams, Mednet has the real-world experience to effectively support your clinical research projects from start to finish.
Our EDC-centric eClinical platform, iMednet, optimizes clinical studies of all types and sizes, across all therapeutic areas – accelerating research with exceptional flexibility, ease-of-use, robust functionality, affordability, and stellar support. Learn more about our strengths
