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.
-For an infographic of all these software solutions, have a look at the Clinical Trial Software Landscape.
-For further insight & resources on the Clinical Trial Software Industry, visit our Content Library.
