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Clinion Named #1 Clinical Trial Management Solution Provider of 2023 by Medhealth Review

Clinion Named #1 Clinical Trial Management Solution Provider of 2023 by Medhealth Review

Austin, TX — November 08, 2023

Clinion has been named the #1 Clinical Trial Management Solution Provider of 2023 by Medhealth Review, recognizing the company’s leadership in advancing clinical trials with cutting-edge AI-enabled technology.

This recognition highlights Clinion’s commitment to a fully integrated eClinical platform that combines EDC, IWRS/RTSM, CTMS, ePRO, eConsent, CSR Automation, eProtocol Automation, and AI Medical Coding into a single, seamless system.

Clinion’s eClinical Platform harnesses artificial intelligence to generate actionable, data-driven insights that optimize study protocols and support informed decision-making. Designed to facilitate decentralized trials, it enables participants to engage remotely, improving accessibility and flexibility. With real-time monitoring, robust security, and seamless team collaboration, Clinion provides a unified solution covering every stage of a clinical trial, from start-up through close-out.

This recognition reaffirms Clinion’s mission to advance clinical research, accelerate trial timelines, and bring new therapies to patients more efficiently. It also reflects the dedication of Clinion’s team and the support of its clients, which have been instrumental in driving innovation in eClinical solutions.

Read The Full Story Here

If you are interested in learning more about Clinion and our innovative clinical trial management solutions. Contact us today.

MANUJ VANGIPURAPU

 

About Clinion

Clinion’s AI-enabled eClinical platform delivers a unified suite of solutions – EDC, RTSM, CTMS, eConsent, ePRO, eSource, eProtocol Automation, CSR Automation, and Document Automation – designed to drive efficiency, ensure continuity, and enable intelligent automation across the entire clinical trial lifecycle. Committed to innovation through AI and ML, Clinion empowers its partners to conduct smarter, faster, and more cost-effective trials.

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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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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.