Older man smiling while reviewing eConsent on mobile phone, with YPrime eConsent platform screens showing consent notification and patient sign-in.

Electronic Consent (eConsent)

eConsent for Clinical Trials. Start Enrollment with Confidence.

Enrollment delays remain one of the most persistent challenges in clinical research. Nearly 40% of all trial spend is tied to recruitment, and more than two-thirds of sites fail to meet enrollment goals.1 For sponsors and CROs running global clinical trials, electronic consent plays a critical role in accelerating enrollment when it is designed for real-world participant and site use.

YPrime’s eConsent for clinical trials is purpose-built to support both enrollment and ongoing protocol changes, helping sponsors and CROs reduce friction for participants and sites while maintaining regulatory confidence from first consent through study closeout.

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Make Clinical Trial Enrollment Seamless with eConsent.

YPrime’s eConsent for clinical trials streamlines the informed consent process by combining intuitive design, global compliance support, and in-house assistance for participants and sites. Our electronic informed consent solution helps teams improve participant understanding, reduce enrollment delays, and support site workflows with consistency and confidence.

The result is a faster, more reliable trial startup, without compromising regulatory expectations or data integrity.

Get Started    

Make Enrollment Seamless with eConsent.

YPrime’s eConsent for clinical trials streamlines the informed consent process by combining intuitive design, global compliance support, and built-in assistance for patients and sites.Our electronic consent solution helps clinical trial teams improve participant understanding, reduce trial enrollment delays, support clinical trial sites, and more. The result is a faster, more reliable start to your trial—without compromising regulatory expectations.

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Simplify Clinical Trial Enrollment with an Advanced eConsent Platform. 
Computer screen icon displaying pie chart and bar graphs, representing dynamic clinical trial information for clear data visualization and communication

Present
dynamic trial
information

Deliver interactive, multimedia consent content that clearly explains trial requirements, expectations, and risks—supporting truly informed consent.

Icons of computer, tablet, and mobile phone representing patient support across all devices, in any language and at their own pace

Support your
patients on
any device

Enable participants to review and complete electronic consent on mobile, tablet, or desktop devices, in their own language and at their own pace.

Headset and chat bubble icon representing built-in patient support for clinical trials, available whenever assistance is needed

Deliver
immediate,
built-in support

Provide real-time access to assistance during the consent process, reducing delays, minimizing site workload, and preventing incomplete or incorrect submissions.

Enhance Clinical Trial Integrity with Secure, Compliant eConsent.

Regulatory requirements for electronic consent continue to evolve across regions. YPrime’s eConsent platform is designed to support compliant, ethical informed consent across global clinical trials, helping sponsors and CROs remain inspection-ready at every phase of the study.

Secure, encrypted data storage
Complete version history and audit trails
Inspection-ready documentation for regulatory review
Female patient electronically signing a consent document on a smartphone, representing streamlined eConsent in clinical trial technology
Clinician using a tablet to manage electronic consent, ensuring clinical trial data integrity and regulatory compliance

Re-Consent Without Disruption.

Paper consent and manual re-consent workflows slow trials down, especially when protocols change. Missed signatures, outdated versions, and manual tracking introduce unnecessary risk for sites and sponsors.

YPrime eConsent transforms re-consent into a seamless digital workflow. New consent versions are deployed instantly while outdated forms are automatically retired. Only impacted participants are flagged for re-consent, allowing sites to focus effort where it matters most. Progress is tracked in real time with complete audit trails, and participants can clearly see what has changed, review updates, and re-sign from any device, anywhere.

The result is faster, smarter consent and re-consent management, without confusion, compliance gaps, or operational disruption across global clinical trials.

At YPrime, data security is at our core. All data in our platform is encrypted, and every version change is stored for future compliance needs or audits.
– David Wallace, Chief Technology Officer, YPrime

Solve Enrollment Challenges
with Certainty.

When we work together, you gain confidence that your clinical trial consent process is compliant, efficient, and designed for both patients and sites. Let’s simplify enrollment, and start trials stronger.

Explore Insights from Our Experts.

Gain valuable perspectives on clinical trial consent, participant engagement, regulatory readiness, and operational execution—so you can run your clinical trials with certainty.

Sources:

1Considerations For Improving Patient Recruitment Into Clinical Trials

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