Easy to use, powerful, and secure
Clinical Trials platform.

Collect and manage data on a unique next-generation EDC platform. Improve data quality and save time. Offer a unique experience for Sponsors, CROs, and patients with our eCRF, ePRO, eConsent, and eConsult solutions.

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International companies trust us

Our solutions

Modular and flexible solutions for your next on-site or decentralized clinical trials.

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eCRF EDC

Build your own studies and forms within minutes, use a next-generation builder. Collect and manage data in real-time from any device and at any time with our modern, compliant, and flexible EDC/eCRF Platform.

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ePRO

Eliminate paper forms and increase subject engagement with our ePRO. Build surveys, and collect data from anyone whether they’re sitting across the room, or across the globe using different devices (tablets, phones, computers…).

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eConsent

Offer a unique experience and reduce the Informed Consent process by more than 50%. Start studies faster, accelerate subject recruitment, and benefit from interactive and secure electronic consent solutions for your studies.

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eConsult

Conduct your clinical trials hybrid or remotely with our eConsult solution. Pre-screen, Screen, Enroll, Evaluate… Use our modular platform for your decentralized clinical trial link to our eCRF. Collect data in real-time.

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By Industries

Flexible platform for you and your company

CROs

Save time and money with our next-generation EDC platform. Easily set up, collect, and manage high-quality data from any device, at any time.

MedTech

Efficiently capture high-quality data and manage medical device and diagnostics trials. Easily comply with all regulations (EU-MDR, CE Mark, FDA…), save time and costs.

Cosmetics
& Personal Care

Reduce time spent building and managing your clinical tests. Manage all your data in a unique and flexible platform with 100% autonomy.

Hospitals & Academic

Easy-to-use, flexible, secure, and affordable platform for your studies. Create and set up your own studies within minutes and without any technical skills.

4,500
Studies completed on Datacapt
60
Improve quality and sponsor trust
65
Countries & 10+ languages

Save time at every stage of your clinical trials with Datacapt!

Halve the time spent setting up, collecting, managing, and processing your clinical trial data. Take advantage of a single, secure, and compliant platform to collect on-site or decentralized clinical data. Our EDC, eCRF, ePRO (Surveys), and eConsent (Electronic Informed Consent) and eConsult (Televisit) allow you to take your clinical trials to the next level. Save time and cost with a flexible, and easy to use features. It is simple, fast, and automated.

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Enjoy a compliant and 100% secure solution

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Why choose Datacapt?

Simplify the management of your trial with the Datacapt platform. Developed with specialists and experts, our platform is flexible and adapted to your studies. We offer a modular platform with everything in one place to design and manage all your trials (EDC, eCRF, ePRO/eCOA/eDiary, eConsent, eConsult, and Data Analysis…).

  • Global and secure Platform (GDPR, FDA 21 CFR PART 1, HDS, ISO 27001…)
  • Modern and easy to use interface
  • Review and monitor your studies with real-time reports
  • Quickly build your forms (eCRF, ePRO, eConsent…)
  • Modular and flexible platform for simple or complex studies
  • Scalable and powerful for all your projects
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On average, our customers are more productive...

40
Reduction of forms construction time such as eCRF, ePRO
85
Have better visibility over their clinical studies and data
100
Day-to-day user satisfaction

“The Datacapt platform allows us to optimize our studies management, with quality and safety assurance. We built our eCRF rapidly according to our own procedure. We can monitor the progress of ongoing clinical trials in real-time, and save time on data management and analysis.”

Louis LétinierSynapse Medicine

“We chose Datacapt for one main reason: it is a modern global platform. Datacapt’s advantage is their availability and responsiveness. When questions or problems arise, we are sure to get a quick response from them.”

Yolande JimenezComplife Group

a better clinical trials management⚬

a better clinical trials management⚬

a better clinical trials management⚬

a better clinical trials management⚬

a better clinical trials management⚬

awaits you with Datacapt⚬

awaits you with Datacapt⚬

awaits you with Datacapt⚬

awaits you with Datacapt⚬

awaits you with Datacapt⚬

Choose Datacapt for your next clinical trials.

Discover our Datacapt Platform and see how we make it easy to build, manage and conduct your clinical trials.

Try out Datacapt