Datacapt EDC eCRF Clinical Trial Software

Electronic Data Capture
for Modern Clinical Studies

Datacapt EDC eCRF makes it easy to build studies, collect, validate, and manage clinical trial data from any source.
Designed for all types of protocols, build studies in days, ensure cleaner data, and save significant time and effort.

Electronic Case Report Form
Clinical Data Management
Intuitive and Flexible
Secure and Compliant

Our user-friendly platform is trusted worldwide for clinical study data management

Tired of data management headaches?
Rethink What an eCRF Can Be.

Modern clinical trials demand more than legacy tools patched for the future.
Datacapt eCRF is a cloud-native, intuitive, and AI-assisted solution designed from day one to empower data-driven research.
From first visit to last patient out, your teams move faster, with fewer clicks, cleaner data, and no tech headaches.
Study Design

Build without limits

Datacapt empowers every teams with a visual builder, enabling them to design and launch studies quickly, all without requiring technical expertise.

Build and deploy studies faster

Preview and test in real-time with zero code

Create complex forms with +25 questions types

Advanced field logic for conditional visibility and validation rules (edit checks)

Everything you need to design, and more (visual builder, real-time preview, form library, CDISC compliance, API)

Collect Clinical Data

Stay Ahead with Study Insights

Simplify data entry with the most intuitive eCRF interface. Experience the power of our user-friendly interface, revolutionizing your data collection process like never before.

Sites enter data quickly with smart autofill and skip logic

Any Role, One Interface

Integrate with all sources (EHR, ePRO/eCOA, Wearables and much more)

Export standardized data anytime in various formats, including CSV, XLSX, PDF, and SAS.

Monitoring & Real-Time Overview

Get cleaner data with less effort

Gain a comprehensive view of your study’s progress with real-time monitoring tools. Monitoring is a critical mission in clinical trials, ensuring data quality, regulatory compliance, and successful study execution.

Get an overview of Data Entry Progress and Study Statistics

Track and resolve queries efficiently with integrated workflows

Access +15 Comprehensive Reports

Review, Source Data Verification (SDV), Lock, and Sign your Clinical Data with Ease.

See why Datacapt
goes beyond
traditional EDC

Experience how Datacapt redefines clinical data collection.

Datacapt isn’t a legacy system, it’s the next generation.

Everything you need and more

Packed with powerful features, 100% cloud and secure.

Frequently asked questions

What is Datacapt EDC?

Datacapt EDC is an electronic data capture application that allows CROs, Sponsors and Academic Research to design and build data collection forms and enables patient data collection from sites efficiently and securely.

Do I need technical skills to build or manage an eCRF?

Designing eCRFs is intuitive and 100% no-code with a visual builder. No technical skills are needed, and you can use pre-built templates or customize forms effortlessly to suit your study.

Is Datacapt 21 CFR Part 11 Compliant

Yes, Datacapt is fully compliant with 21 CFR Part 11 and other data privacy regulations. It’s fully validated, auditable, and audit-ready at all times. Validation documentation is available on request.

Are audit trails and electronic signatures part of the system?

Yes. Every data entry, change, and user action is audit-trailed in real time. Electronic signatures are Part 11-compliant, timestamped, and fully traceable—meeting all regulatory expectations.

How secure is the data in your EDC/eCRF system?

Your data is protected using end-to-end encryption—both at rest and in transit. We use AES-256 encryption, secure HTTPS protocols, and enforce strict data access policies across the platform. Data is hosted on ISO 27001-certified cloud infrastructure with geographic redundancy.

How does role-based access work in your eCRF?

You can assign roles and permissions at a granular level, from data entry and monitoring to database lock and export. Each user only sees the data and features they need, ensuring security and clarity.

What export formats are supported?

We support exports in CSV, Excel, PDF, and SDTM formats. You can export data on-demand at any point. Exports are secure, audit-logged.

How long does it take to launch a study with Datacapt?

Most studies can be built and deployed in less than one weeks using our form builder and template libraries.

📞 Ready to Experience It?

What do customers say about Datacapt ?

Find out why 200+ companies place their trust in the Datacapt
Platform to manage their clinical trials.

"When I first opened Datacapt, I instantly got the feeling this was the next generation of eClinical platform!"
Jakub Poplawski
Global Dir. Business, Zurko Research
"Thanks to Datacapt, we cut our site training time by four, reduced setup timelines by 40%, and boosted both our processes and responsiveness."
Chloé Arnous
Clinical Project Manager, Ceiso
"Datacapt surpassed our expectations thanks to its user-friendly interface ans the availability of its team. It made form design and data collection remarkably intuitive resulting in significant time savings and enhanced accuracy."
Axel Boulet
Data Steward, Owkin
"Datacapt is a reliable and educational tool, designed to support researchers at every stage of their clinical study, with easy handling and high-quality service."
Prof. Laurent Calvel
Head of the Palliative Care Dpt, Hospital of Strasbourg
"By trusting Datacapt, we quickly achieved a level of regulatory compliance we couldn’t have reached on our own, while gaining autonomy in our clinical studies."
Samuel Lerman
Co-founder, Emobot
"The intuitive interface allowed us to structure operations and launch our business in under two months"
Jade Beaumont
HDRS Laboratory Manager, Weneos

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