iMednet eConsent

The iMednet eConsent system simplifies the participant consent process by providing a secure and efficient electronic informed consent solution integrated within the iMednet platform. It allows study participants to review and provide consent at their convenience, using any device such as smartphones, tablets, or laptops, thanks to its responsive design.

Seamless Consent Tracking

The platform includes a dashboard that enables site users to track the consent status, ensuring compliant collection and storage of electronic signatures along with the date and time of consent. This feature provides visibility into the current status of consents and access to completed consents.

Participant-Centric Access

iMednet eConsent offers a participant-centric approach, breaking down geographical barriers and saving time by allowing researchers to connect with potential participants globally.

Flexibility and Customization

The system is highly flexible, allowing participants to choose between electronic or paper consent. Study designers can customize the consent flow, including multiple page designs to make the consent process more manageable. Additionally, the wording on the consent form can be tailored for the Institutional Review Board (IRB) at each site.

Engagement and Education

Participants' understanding is enhanced through embedded media support, such as videos or graphics, which describe study protocols, potential risks, benefits, and the consent process.

User-Friendly Guidance

An intuitive interface guides participants through each section of the consent, ensuring all critical information is covered.

Compliance and Security

iMednet eConsent employs robust security measures to protect sensitive participant information, maintaining compliance with industry regulations like HIPAA and GDPR.

Overall, iMednet eConsent offers a customizable solution that combines functionality, flexibility, and affordability, supporting a wide range of study types and phases.