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Clinical Trial Software, Clinical Trial Management System, illustration, CTMS, etmf, EDC, ePRO

What is eConsent Software?

eConsent software is used to manage the informed consent process digitally in clinical trials. It allows participants to read, review, and sign consent forms on a tablet, smartphone, or computer. The software includes videos, quizzes, and other tools to help patients understand the study before agreeing to take part. This improves clarity and helps ensure that consent is truly informed.

Researchers use eConsent to track who has signed, when they signed, and whether they understood the key parts of the study. The system stores all records securely and keeps a clear audit trail. It also reduces paperwork and supports faster startup times. eConsent software is widely used in both site-based and decentralized trials.

 

All eConsent

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Datacapt eConsent

Opt for an innovative digital solution that simplifies access to clinical studies, improves patient understanding and ensures smooth, informed consent that complies with international standards (GDPR, FDA 21 CFR Part Read More...
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Replior eConsent

Replior’s eConsent simplifies participant onboarding and ensures compliance, supporting clinical trials with an accessible, transparent, and reliable consent process. Securing informed consent isn’t just another task. It’s a critical step Read More...
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Datacubed eConsent

Improve Patient Understanding and Reduce Dropout Our built-in Electronic Consent (eConsent) facilitates a consent process that includes providing study information to participants, evaluating participants’ comprehension of the information presented through Read More...
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Research Manager eConsent

Participant engagement is key to the success of a clinical trial. ResearchManager eConsent positively encourages participant engagement and participation while maintaining the integrity of the study. Instead of cluttered paperwork Read More...
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Delve Health eConsent

BENEFITS OF CLINICAL TRIAL eCONSENT INCLUDE, BUT ARE NOT LIMITED TO. eConsent is improving clinical trials by offering a digital, user-friendly approach to obtaining patient consent.This transformation offers numerous benefits, Read More...
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Clinical Trial Services Solutions Sitero 3

Sitero MENTOR eConsent

Consent forms are one of the first and most important patient touch points. Sitero’s unique eConsent offering is adaptable and made for modern clinical trials. It is designed to meet Read More...
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dfNet eConsent

Improve clinical study recruitment with a patient-centric eConsent solution DFconsent engages participants with interactive multimedia in their local language so they can make informed decisions about their participation in your Read More...
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Suvoda eConsent

Ease of understanding for patients. Full visibility and automated control over the consent process for sponsors. Extend your clinical trial command and control center with Suvoda eConsent. Improve patient comprehension. Read More...
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5th Port eConsent

Engage patients in a meaningful and fully documented eConsent process. 5thPort’s patient education and eConsent solution allows patients to ask questions, flag sections for further clarification, and provide consent in Read More...
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DSG eCaseLink eConsent

Secure, flexible, and convenient data capture eCaseLink eConsent can be used as a standalone or part of the fully harmonized unified eCaseLink EDC platform. It captures participant data conveniently on-site Read More...
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Top benefits of eConsent software:

  • Better patient understanding: Interactive content helps explain study details clearly.
  • Faster enrollment: Patients can complete consent forms remotely and on their own schedule.
  • Reduced errors: The software checks for missing signatures or unanswered questions.
  • Secure recordkeeping: Digital signatures and audit trails improve data integrity.
  • Easier tracking: Researchers can see consent status in real time for each participant.
  • Supports remote trials: Patients do not need to visit a site to give consent.
  • Improved compliance: Built-in checks help meet regulatory and ethical standards.
  • Multilingual options: Consent forms can be shared in different languages to support diverse populations.

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