ACCMED-IRT

Harnessing industry-leading microservices and cloud-native architecture, ACCMED-IRT empowers you to create customized workflows for study design, randomization algorithms, and subject management, significantly streamlining library development for complex clinical trials.

With the largest clinical trial delivery team in Asia-Pacific region, ACCMED-IRT has been proven excellence through 100+ global inspections, backed up by over 1,500 successful clinical studies. Our platform offers a robust standard configuration, seamlessly integrated with professional-grade customized services to ensure precise support for every type of trial.

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Core advantages
of the product

Powerful products and Proven Expertise

Forged through years of continuous innovation and deep industry insight, ACCMED-IRT delivers a powerful, ready-to-deploy standard configuration—honed through real-world application and high-end customization. Whether your trial is simple or highly complex, ACCMED-IRT is designed to adapt and perform. With seamless bidirectional integration across global clinical systems—including EDC, eCOA, CTMS, WMS, and Lab—ACCMED-IRT helps you streamline operations and accelerate your path to trial success.

Industry-leading technology accelerates go-live efficiency

ACCMED-IRT is built on a modern microservices and cloud-native architecture, integrating powerful engines for configuration, workflow management, and computation. It supports fully customizable study setups, including advanced randomization algorithms and subject management capabilities. Designed to handle complexity with ease, ACCMED-IRT delivers rapid, reliable database creation—even for the most demanding protocols—helping sponsors and CROs shorten timelines and scale with confidence.

Accurate Drug Prediction and End-to-End Traceability

The increasingly complex study design and changing operational requirements pose a significant challenge for clinical drug supply management. ACCMED-IRT addresses this through its unique patented algorithms coupled with full-link drug traceability, providing complete visibility for each drug. Combined with rich drug supply strategies, ACCMED-IRT simplifies drug supply management from design to execution.

Global best practices

Backed by a 100% audit pass rate from both domestic and international regulatory agencies and industry leaders, our products and services embody the highest standards of reliability and compliance.

Transform Your
Clinical Trials
with ACCMED-IRT

Smarter Randomization. Optimized Supply. Faster Trials.

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