Build forms, collect, monitor, share and manage clinical data on our next-generation eClinical platform (EDC). Improve data quality and save time. Offer a unique experience to Sponsors, CROs, and patients with our eCRF, ePRO, eConsent, and eConsult solutions.
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
Enjoy a compliant and 100% secure solution
On average, our customers are more productive...
“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