Explore the Largest Directory of Software Solutions for your Clinical Trial Needs

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

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.

Ready to take the next step?

Request Information, Proposals or Quotes from vendors