eClinical Solution for Contract Research Organizations

The CRO's Trusted Clinical Data Partner

Accelerate every study with a flexible, scalable platform built for Contract Research Organizations. From customizable eCRFs to real-time insights, Datacapt adapts to your most complex trial requirements.

Get a demo

Join a Powerful Community Driving Change thanks to Datacapt

Why CROs Choose Datacapt

Power up your CRO operations with unified tools that accelerate study start‑up.
Ensure data integrity, and keep every stakeholder in sync.

Speed Up Timelines

Launch studies in days, not weeks. Our unified platform and drag‑and‑drop eCRF builder get you live faster with everything you need.

Boost Data Quality

Smart edit checks, query management, and audit trails ensure you hit clean‑data milestones every time.

Streamline Collaboration

Role-based access and real-time dashboards keep sponsors, sites, and monitors aligned with the right data, at the right time.

Using Datacapt means showing the image of a company that is moving forward.

Christine Perrier-Gillioën

Quality Assurance Director

Clinical Trials

Built for CROs Excellence

Run exceptional trials on a platform that grows with you. Trusted in 50+ CRO-led studies worldwide, Datacapt blends regulatory strength with seamless usability.

Learn More

60%

Faster study setup

Spend less time configuring and more time enrolling.

99.9%

System uptime

To keep your trials running. Zero disruption, full confidence.

Comprehensive Modules
‍Designed for CROs

From eConsent to data collection and monitoring — Datacapt’s modular platform supports your study from start to finish.

eCRF

Capture clean, compliant, and high-quality clinical data with an intuitive and customizable electronic Case Report Form

ePRO

Collect real-time patient-reported outcomes through user-friendly digital interfaces that boost engagement and compliance.

eCONSENT

Simplify the consent process with digital, compliant, and patient-friendly eConsent forms that streamline onboarding.

Recruitment

Accelerate patient recruitment with built-in tools that help you identify, screen, and enroll the right participants faster.

Scheduling

Easily manage site visits and patient appointments with automated scheduling tailored to your study timelines.

Patient Payments

Ensure timely, transparent compensation with automated patient payments that build trust and reduce administrative burden.

FAQs

Can Datacapt manage multiple studies and teams concurrently?

Yes. Our Unlimited Studies plan lets you run as many parallel trials as you need, with granular role‑based permissions to keep data secure.

Can we manage multiple studies and sponsors on one account?

Yes. Datacapt supports multi-project and multi-sponsor management, allowing CROs to easily switch between studies and customize access per client.

Can we build studies ourselves, or do we need your team?

Yes, you can build studies independently using our intuitive no-code tools. For teams that prefer support, our services team can assist with study setup, data management, or migration.

Is Datacapt compliant with industry regulations?

Absolutely. Datacapt is fully validated and compliant with GCP, 21 CFR Part 11, GDPR, and HDS. Full audit trails are included at both platform and study levels.

Does Datacapt support multi-country or multi-site studies?

Yes. Datacapt is designed for global trials, with tools to manage multiple countries, languages, sites, and roles.

What kind of support is available during the study?

We offer dedicated support with rapid response times, onboarding assistance, and optional full-service packages including study build, data monitoring, and close-out.

Our customers
say it best

Our customers are running faster, smarter clinical trials and we’ve documented how. Real teams. Real timelines. Real impact.
And maybe… your next move?

Read the stories

The CRO's Trusted Clinical Data Partner