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Greater participation, and improved data quality.

On-site, hybrid and
remote eConsent.

Experience faster and improved patient recruitment with eConsent. Upgrade to eConsent, streamlined processes grant better access to studies while enhancing patient engagement, ensuring a seamless and informed consent experience.

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Utilizing eConsent modernizes and enhances the informed consent process, ultimately benefiting both participants and researchers.

Better
informed

eConsent engages participants with multimedia, simplifying complex information. Participants navigate content at their pace, leading to improved informed decision-making.

Accelerate
enrollment

eConsent streamlines comprehension, signing, and tracking, reducing manual handling. It simplifies both the review and enrollment processes.

User-Friendly
interfaces

Datacapt eConsent provides intuitive interfaces, interactive elements, and guided navigation for easy participant comprehension and user-friendly step-by-step processes.

Gain real-time visibility
across all your sites

Real-time tracking and monitoring empower coordinators to guide patients through enrollment stages, ensuring compliance and timely support. Enhanced engagement aids adherence to regulations, fostering well-managed clinical trials.

A simple
user experience

Accessible from any device (BYOD) Datacapt eConsent ensures a seamless experience anywhere in the world. Participants effortlessly review, sign, and engage with consent materials, enhancing accessibility and convenience in the process.

Hot

Televisits for remote eConsent

Televisits enable remote eConsent, allowing participants to review and sign consent forms from any location, enhancing convenience, accessibility, and study enrollment efficiency.

User management

Introducing adaptable roles to streamline consent workflows and manage multicenter studies efficiently. Choose custom or predefined roles: Study Admin, Data Manager, Site Admin, Investigator, Monitor, Read-only users.

Compliance

Designed to comply with global regulations, including FDA 21 CFR Part 11, ICH GCP, and GDPR, eConsent digitizes and secures consent processes for accuracy, accessibility, and auditability.

Need more info?
Check out our most frequently asked questions.

What is eConsent?

eConsent digitizes and streamlines informed consent, enabling participants to electronically review, sign, and engage with study materials, enhancing accessibility and precision.

What signature options are available?

Datacapt provides three types of eConsent signatures: a digital 21 CFR PART 11 compliant signature, an eSignature (eIDAS compliant), and support for wet-ink signatures.

Can I utilize eConsent for a multinational multi-center study?

eConsent enables streamlined multi-center studies across diverse countries. Its digital adaptability ensures seamless participation, compliance, and enhanced study efficiency and reach.

Is on-site eConsent possible?

Datacapt offers a user-friendly on-site and in-person eConsent signature option, ensuring a quick and convenient process.

Start Your Journey with Datacapt eConsent

Boost Enrollment Efficiency with Datacapt eConsent.

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