Your Clinical Data Technology Partner: Better Studies, Together.
State-of-the-art EDC and ePRO solutions to collect, manage, and analyze clinical data efficiently while ensuring full regulatory compliance.
The Clindox Difference
Market-proven technology to meet global regulatory and business objectives.
Reduce Time to Market
Study setup in days, not months. We build it for you, or you build it yourself.
Versatile Data Capture
EDC, ePRO, or eDiary—data collection on any device, intuitive and integrated.
Secure & Compliant
Market-proven technology to meet global regulatory and business objectives.
Human Support
Direct access to trained experts who prioritize your study's success.
Core Products
Everything you need to run efficient, compliant clinical studies in one unified platform.
eCRF
Streamlined Electronic Case Report Forms for trial efficiency.
ePRO & eDiary
Integrated subject-led data collection on any device.
MedDRA Coding
Built-in regulatory dictionary coding for safety data.
Randomization
Simple, block, and stratified randomization options.
Proven for Medical Device Investigations
Helping companies meet IVDR and business compliance requirements with cost-effective, market-tested EDC solutions.
Social Proof
Trusted by clinical trial leaders around the world.
"The Clindox team have been an incredible support to us throughout our study setup and execution. The platform is robust and highly flexible."
Maria Galligan
PMD Solutions
"The time and cost saving is significant. I wouldn't hesitate to recommend it. Clindox provides a state-of-the-art solution for clinical researchers."
Dr. Salvi
India
Seeing is believing.
Request your personalized demo today and experience the future of clinical data technology.