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.
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Why Pharma & Biotech Teams Love Datacapt
Move fast. Launch smarter.
Unlock Real‑Time Insights
Ensure Regulatory Readiness

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.

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.
Faster site activation
Launch studies in days, automate builds and deploy at scale.
Compliance-first, always
Stay aligned with global regulations with built-in, audit-ready controls.
Core Modules for
Pharma & Biotech Teams
Capture clean, compliant, and high-quality clinical data with an intuitive and customizable electronic Case Report Form
Collect real-time patient-reported outcomes through user-friendly digital interfaces that boost engagement and compliance.
Simplify the consent process with digital, compliant, and patient-friendly eConsent forms that streamline onboarding.
Simplify setup, support complex designs, and ensure balanced treatment allocation with zero manual effort.
Track inventory, shipments, and site stock levels in real time to avoid shortages and streamline your study operations.
Real-time coding integrated in your EDC ensures faster submissions, consistent data, and reduced query cycles.
Frequently Asked Questions
Most teams are onboarded and ready to launch their first study in just a few days, thanks to our intuitive interface and expert support.
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.