clinion

#1 Award Winning eClinical Platform

Real AI.
Real Impact.

Bringing faster, more accurate, and cost-effective outcomes with AI

Clinion recognized with multiple prestigious industry awards, including the SCDM Innovation Award 2024, ACDM Innovation in the Management of Clinical Data Award 2025, Frost & Sullivan Best Practices Award 2024, Clinical Trial Arena Excellence Award 2024, and Citeline Award 2025 for excellence and innovation in clinical data management and eClinical technology.

Why Us

Integrated. Intuitive. Intelligent

Our platform empowers sponsors and CROs to operate with unparalleled speed, efficiency, and precision. Turning complexity into clarity and opportunities into success, Clinion sets a new standard for smarter and faster trials.

Proven Expertise

Challenging the Status Quo in Clinical Trials

Patients

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Clinical Trials

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Our Products

Explore Our Latest Products

eProtocol

Clinion’s AI auto-generates ICH M11 and TranCelerate-compliant protocol drafts from study summaries in minutes. Automate the entire process of draft generation, collaboration, review, and finalization on a single platform. Reduce costs and timelines by 60%, and ensure greater accuracy with human-guided validation.

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EDC

Clinion EDC is built with AI at its core, not as an add-on. Automate key steps of your study, including Study Setup, CDASH mapping, Remote Source Data Verification, AI Medical Coding, Data Review, and Custom Reporting, with intelligent modules that work seamlessly together. Clinion EDC is built to accelerate trials, with greater efficiency and quality at reduced costs.

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RTSM

Clinion RTSM redefines randomization and supply with industry’s best integration. Automate patient randomization, kit assignment, reassignment, and returns through Clinion EDC without logging into multiple systems. Deploy in days, reduce costs, and ensure accuracy and compliance. Designed for flexibility, Clinion RTSM supports studies ranging from the very simple to the highly complex.

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eConsent

Clinion eConsent simplifies Informed Consent with multimedia forms, real-time tracking, and a patient-friendly UX. Subjects can consent onsite or remotely, with a quick and easy setup experience. Integrated into Clinion EDC, it gives sites a single application to manage both onsite and remote eConsent. Enhance patient understanding, reduce site burden, and shorten setup timelines.

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ePRO

Clinion ePRO is a robust application that can be used as a stand-alone app or integrated with Clinion EDC. Easy to set up, install, and use with real-time updates, it simplifies patient-reported data capture through multilingual forms, automated reminders, and seamless EDC integration. Mobile, tablet, or web entry boosts compliance, slashes setup time, and scales easily for global trial success.

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eSource

Clinion ePRO is a robust application that can be used as a stand-alone app or integrated with Clinion EDC. Easy to set up, install, and use with real-time updates, it simplifies patient-reported data capture through multilingual forms, automated reminders, and seamless EDC integration. Mobile, tablet, or web entry boosts compliance, slashes setup time, and scales easily for global trial success.

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CTMS

Gain complete trial oversight with a centralized CTMS that unifies project tracking, monitoring, and financials. Integrated with EDC and RTSM, it delivers real-time visibility and operational clarity for CROs and sponsors.

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CSR

Generate high-quality CSRs with AI that extracts key insights from the Protocol, SAP, and TLFs, auto-populating up to 70% of the CSR while ensuring ICH E3 compliance. Cut timelines, reduce manual effort, and maintain full oversight and accuracy.

eTMF

Streamline trial document management with pre-built DIA models, real-time tracking, and version control. Ensure compliance, enable bulk uploads, and stay inspection-ready with robust audit trails across the trial lifecycle.

Awards & Recognitions

Achievements in Clinical Excellence

Clients Testimonials

What Our Customers Say About Our Services

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

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