eCONSENT
Our eConsent module transforms the traditional paper-based consent process into a fully digital, compliant, and patient-friendly experience.
Designed for clinical trials, research studies, and medical device evaluations, eConsent ensures participants clearly understand the study before giving consent — while sponsors and CROs maintain audit-ready documentation in real time.
With multilingual capabilities, interactive content, and secure authentication, our eConsent helps improve participant comprehension, enrollment speed, and regulatory compliance.
Product Features
Our eConsent module is designed to streamline the entire consent process — from participant education to regulatory compliance — all in one secure platform.
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Boost Recruitment Rates
Make it easier for participants to enroll with remote and on-site signing options. -
Improve Participant Understanding
Use interactive, multimedia consent forms to clarify study expectations & risks -
Ensure Regulatory Compliance
Fully compliant with FDA 21 CFR Part 11, HIPAA, GDPR, and ICH-GCP.
Simplify, secure, and speed up your consent process today.
📅 Book a Demo or 📥 Download our eConsent brochure to learn more about how we help clinical teams achieve faster, safer, and more patient-friendly consenting.
1. Is the eConsent legally valid?
Yes, our eConsent complies with FDA 21 CFR Part 11, HIPAA, GDPR, and e-signature laws worldwide.
2. Can patients sign remotely?
Yes, remote consent is fully supported via secure web links and authentication.
3. Does it support multimedia content?
Absolutely. You can include videos, images, and interactive elements in consent forms.
4. How do we ensure participant comprehension?
You can embed quizzes, information checks, and interactive FAQs to confirm understanding.
5. Can it integrate with our EDC and CTMS?
Yes, we offer seamless integration with major clinical trial management and data capture platforms.