Clinion

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Clinion's AI-enabled eClinical platform integrates EDC, RTSM, CTMS, eConsent, ePRO, eSource, eProtocol Automation, CSR Automation, and eTMF to streamline clinical trials. Our advanced AIML and GenAI modules accelerates trial timelines, enhances compliance, and reduce costs, making trial management seamless and efficient.

Clinion’s award-winning AI and GenAI-enabled eClinical platform provides a comprehensive suite—EDC, RTSM, CTMS, ePRO, eConsent, eSource, eProtocol, CSR Automation, and eTMF—designed to streamline and accelerate every phase of clinical trials. Our team consists of pharmaceutical and technology experts who have helped organizations across India, USA and Europe conduct more than 350+ clinical trials,
including several COVID-19 studies. As a product, Clinion is an all-in-one integrated eClinical trial platform for small and medium CROs, academic research organizations and pharmaceutical companies. Clinion enables you to set up and manage clinical trials with an accelerated start, ease of use and high data quality thanks to an integrated Electronic Data Capture (EDC), Randomization and Trial Supply Management (RTSM), Clinical Trial Management System (CTMS) and Electronic Clinical Outcome Assessment (eCOA) supported by AI and Automation.

For more information log on to

www.clinion.com
including several COVID-19 studies. As a product, Clinion is an all-in-one integrated eClinical trial platform for small and medium CROs, academic research organizations and pharmaceutical companies. Clinion enables you to set up and manage clinical trials with an accelerated start, ease of use and high data quality thanks to an integrated Electronic Data Capture (EDC), Randomization and Trial Supply Management (RTSM), Clinical Trial Management System (CTMS) and Electronic Clinical Outcome Assessment (eCOA) supported by AI and Automation.

For more information log on to

www.clinion.com

03/11/2026

What can you achieve when your EDC does more than capture clinical data?

From accelerating study setup to generating custom reports with AI, supporting CDISC mapping, and improving data review, Clinion’s AI-native EDC brings together capabilities that help clinical teams manage more of the study lifecycle in one connected platform.

With integrated workflows for data management, reporting, and query resolution, teams can move from identifying an issue to taking action without juggling disconnected tools.

And that’s just part of what Clinion EDC offers.

Want to see how it could support your clinical data workflows? Connect with us to learn more. https://www.clinion.com/

28/10/2026

Protocol amendments shouldn't put live studies on hold.

With Clinion EDC, update visits, pages, and fields mid-study without downtime or vendor assistance. Automatic version control protects existing data, while reports stay aligned with the latest CRF version.

0% study downtime. 40% savings in time and costs.
Because a protocol change shouldn't mean starting and stopping your study.

Accelerate your trials with Clinion EDC: https://www.clinion.com/electronic-data-capture-edc-software/

26/10/2026

Patient-reported data collection should be simple and easy to access.

Clinion ePRO captures responses directly from patients and validates them in real time, giving study teams timely visibility into patient-reported outcomes throughout the study.

This helps teams stay closer to patient-reported data as it comes in, making ongoing review more consistent while keeping the experience straightforward for patients.

Discover how Clinion ePRO can support your study.
https://www.clinion.com/electronic-patient-reported-outcome-epro/

23/10/2026

Tomorrow, the Clinion team will be at the ACDM India Summit 2026 in Bengaluru!

We're looking forward to a day of expert insights, knowledge sharing, and discussions on clinical data management.

Attending the summit? Come meet our team, exchange perspectives, and connect with us in Bengaluru.

See you tomorrow!

Learn more about Clinion: https://www.clinion.com/

21/10/2026

The Clinion team will be at the ACDM India Summit 2026 in Bengaluru on 24 October.

From connecting clinical systems to rethinking data review and reporting, we're keen to exchange ideas on the challenges clinical data management teams face and where agentic AI can make a practical difference.

Will you be at the summit? Connect with the Clinion team to share perspectives and discuss what's next for clinical data management.

16/10/2026

What’s next for clinical data management?
The Clinion team will be attending the ACDM India Summit 2026 in Bengaluru on 24 October.

We'll be connecting with clinical data management professionals to discuss how agentic AI can support cross-system data review, custom reporting, and everyday data management tasks.

We'll also share insights into our Agentic Assistant, which connects clinical systems such as EDC, CTMS, and RTSM through a common interface.

Attending the summit? Book a 30-minute session with the Clinion team to discuss the applications of our Agentic Assistant in clinical data management.

https://www.clinion.com/contact/

13/10/2026

Clinical trial data changes throughout a study. Tracking those changes is essential for maintaining data integrity and understanding how the data evolved.

But can AI play a role in audit trail review?
Swipe through to explore why it matters and where AI can help.

Learn more: https://www.clinion.com/contact/

28/09/2026

What if you could move from a study question to the relevant data and queries without switching between clinical systems?

With Clinion's Agentic Assistant, teams can ask questions in natural language, generate custom reports, compare report data, review records, and raise queries across connected clinical workflows.

See how Agentic Assistant brings data, reporting, and Data Review together through a common interface.

Explore Agentic Assistant → https://www.clinion.com/agentic-assistant/

25/09/2026

What if weeks of CSR authoring could be reduced to minutes?

Clinion’s CSR Automation uses GenAI to extract relevant content from the Protocol, SAP, and TLFs and populate structured CSR sections, while keeping medical writers in control of review and refinement.

Explore how AI can simplify CSR generation →https://www.clinion.com/csr-automation/

07/09/2026

Protocol development is changing. Is your workflow keeping up?

At SCDM 2026, our CEO, Manuj Vangipurapu, will discuss how AI is entering the protocol development process, from the initial synopsis to the protocol draft.

His session, “AI in the Drafting of Modern Clinical Protocols,” will explore where AI can support drafting, review, and consistency while keeping scientific judgment and oversight with experts.

📅 September 16, 2026
📍 Breakout Room 305A | Raleigh, North Carolina

Join the conversation on what AI-assisted protocol development could mean for the future of clinical research.

Learn more: https://www.clinion.com/events/meet-clinion-at-scdm-2026-conference/

Address

5900 Balcones Drive, STE 100 Austin TX 78731 Travis County

5900

Opening Hours

Monday	10:00 - 18:00
Tuesday	10:00 - 18:00
Wednesday	09:00 - 18:00
Thursday	10:00 - 18:00
Friday	10:00 - 19:00

Website

https://www.clinion.com/

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