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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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Telemedicine eConsent

Telemedicine eConsent

Our intuitive electronic consent (eConsent) solution facilitates the participation of patients in clinical trials, seamlessly and efficiently. Our CleanWeb global e-Platform integrates eConsent, streamlining interactions between patients, professionals, and healthcare Read More...
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Advarra eConsent

Reduce Audit Findings While Increasing the Quality of Your Consent Process Advarra eConsent is an electronic consenting module for research sites, designed to keep participants engaged, simplify compliance oversight, and Read More...
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eClinPro eConsent

Improved Understanding for Participants: eConsent solutions provide interactive tools such as videos, quizzes, and digital materials. These tools help participants better understand the study, thus improving informed decision-making. Streamlined Consent Read More...
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Trialstat eConsent

Accelerate clinical trial enrollment and maximize protocol compliance by leveraging TrialStat’s comprehensive and immersive eConsent platform. Fully configurable workflows include support for witnesses, assent, re-consent, and the ability for patients Read More...
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Axiom Fusion eConsent

Interactive and flexible Informed Consent Forms (ICFs) for your Patients. Use the Fusion eConsent Portal to capture and store consent, synced to Subject Records. The Fusion Advantage Flexible eConsent with Read More...
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Florence eConsent

Make informed consent easy for you and your participants with secure, efficient, and fully digital workflows for clinical trials. Other vendors promise eConsent solutions, but we’re the only ones that Read More...
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Veeva eConsent

Veeva eConsent provides a digital way to consent clinical trial participants in-person or remotely. Break free from legacy tools and cumbersome paper documents. Give your patients access to a modern Read More...
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Castor eConsent

Castor’s modular eConsent solutions improve clinical trial efficiency—from recruitment and screening to direct data capture and analysis. You can use each virtual component on its own or combine them into Read More...
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IQVIA eConsent

QVIA Complete Consent is the user-friendly, flexible, and feature-rich electronic informed consent solution built to support diverse protocols at a global scale. Deliver highly engaging compliant eConsent Verified through more Read More...
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Zapclinica eConsent

eConsent is an innovative, regulatory-compliant, patient-friendly, electronic consent system for clinical trials. Build a streamlined and compliant consent process Build a multi-page consent walkthrough tailored to the specifics of the 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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