eClinical Solution for Pharma and Biotech

The Pharma & Biotech
Clinical Data Engine

Accelerate drug development with a unified eClinical Platform that supports everything
from first‑in‑human to post‑marketing studies.

Launch Faster
Flexibility
Scalability
Compliance
Cost-Efficient
Real-time data

Join a Powerful Community Driving Change thanks to Datacapt

Why Pharma & Biotech Teams Love Datacapt

Accelerate studies, improve data quality and stay in control every step of the way.

Move fast. Launch smarter.

With intuitive no-code tools, prebuilt templates, and automated workflows, Datacapt helps you move faster, without compromising quality or compliance.

Unlock Real‑Time Insights

Interactive dashboards give your R&D, medical, and safety teams instant clarity — across every site, country, and protocol.

Ensure Regulatory Readiness

Built‑in 21 CFR Part 11, GDPR and HIPAA compliance, audit trails make inspections and submissions seamless.

Based on our positive experience, Median Technologies would definitely recommend Datacapt to other research centers for their clinical trials. The platform's ease of use, real-time monitoring capabilities, and overall benefits make it a valuable tool for research endeavors.

Louis Chapotot
Senior Clinical Project Manager
Clinical Trials

Built for Pharma & Biotech Growth

Whether you're running Phase I trials or global registries, Datacapt adapts to your study — and grows with your pipeline. Chosen by innovative Pharma and Biotech sponsors around the world.

3X

Faster site activation

Launch studies in days, automate builds and deploy at scale.

100%

Compliance-first, always

Stay aligned with global regulations with built-in, audit-ready controls.

Frequently Asked Questions

How quickly can we get up and running with Datacapt?

Most teams are onboarded and ready to launch their first study in just a few days, thanks to our intuitive interface and expert support.

How secure is the platform for handling sensitive clinical data?

Datacapt is built with end-to-end encryption, secure user authentication, and complies with industry standards like GCP and 21 CFR Part 11, ensuring your data is protected at all times.

Other question

Simplify the management of your clinical trials

From study design to database lock, manage everything with ease, no coding, no confusion.

Built for Trials.
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