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Clinion Wins The Clinical Trials Arena Excellence Award for Innovation 2024

Clinion wins the Clinical trials Arena 2024 for innovation

Clinion is proud to be recognized with the Clinical Trials Arena Excellence Award for Innovation 2024. This accolade highlights our leadership in transforming clinical trials through AI-driven solutions that simplify operations and uphold the highest standards of data quality.

 

Why Clinion Stands Out

Advanced AI/ML Integration – Smarter, Faster Trials

Clinion leverages artificial intelligence and machine learning to simplify complex clinical trial processes. Features like intelligent CDASH coding ensure accurate data mapping, built-in data validation strengthens study integrity, and enhanced reporting and visualization help teams make timely, informed decisions.


Unified eClinical Platform – Seamless Trial Management

Our comprehensive platform integrates Electronic Data Capture (EDC), Clinical Trial Management System (CTMS), Randomization and Trial Supply Management (RTSM), and Electronic Patient-Reported Outcomes (ePRO), eConsent, and Document Automation in a single interface. Extensive API integrations with lab systems, eCOAs, eDiaries, and CTMS ensure smooth data exchange, while multi-language support enables global usability.


Precision and Speed – Real-Time Impact

Clinion’s platform is designed for rapid setup and intuitive use, enabling study teams to start trials quickly and manage all aspects efficiently. With global libraries and the ability to implement mid-study changes seamlessly, teams can move through studies faster while keeping data reliable and consistent.

The Clinion Advantage

Reduction in trial costs

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Faster protocol generation

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Faster medical coding

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Why This Award Matters

The Clinical Trials Arena Excellence Award underscores Clinion’s commitment to innovation and excellence in clinical research. For organizations seeking a transformative approach to clinical trials, our AI-powered platform provides a proven solution to streamline workflows, enhance data quality, and accelerate study timelines.

Unlock the Future of Clinical Trials with Clinion.

Cut your trial costs by 35% and accelerate your time-to-market by 30%

Compliance

Fully Compliant with Global Standards

FDA,HIPAA and ISO Logos
ich ,gdpr ,eu compliant logos
Clinion’s adherence to global regulatory standards including FDA 21 CFR Part 11, HIPAA, ISO 9001:2015, ISO 27001:2013, ICH, GDPR, and EU Annex 11.