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Clinion

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CTMS for sponsors and CROs with protocol deviation management built in

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  • Deployment Cloud Based
  • Starting price Custom
  • Free trial Not offered
  • Best for SMEs, Enterprises

What is Clinion?

Clinion's CTMS covers Phase I through IV trials for sponsors and CROs, and its most developed capability is protocol deviation management , comprehensive deviation capture, centralised tracking and notifications, aimed at protecting trial integrity by catching problems while they can still be addressed rather than at database lock.

Real-time milestone tracking sits alongside it, keeping delivery timelines visible as the study runs. Clinion emphasises deep integration with its wider suite, simple setup and ease of use, which positions it against enterprise platforms whose configuration cycles can take months. For sponsors and CROs that want deviation oversight without a lengthy implementation, that combination is the argument. Pricing is quoted.

Key Features of Clinion

  • Manage trials across Phase I to IV
  • Capture protocol deviations comprehensively
  • Track deviations centrally with notifications
  • Protect trial integrity through early detection
  • Track study milestones in real time
  • Integrate deeply with the wider Clinion suite
  • Set the system up without long configuration
  • Support sponsors and CROs
  • Monitor site activity and progress
  • Keep delivery timelines visible throughout

Clinion Pricing

Custom

Custom

Quoted per study portfolio

Clinion publishes no pricing. Quotes reflect study volume and which products in the integrated suite are taken alongside CTMS.

Clinion Specifications

Deployment
  • Cloud Based
Billing cycle
Monthly
Desktop
  • Web App
Languages
  • English
Built for
  • SMEs
  • Enterprises
Support
  • Email
  • Live Support
  • Training
  • Tickets
Integrations
Clinion EDC and eClinical suite, eTMF, safety systems
Public API
Yes
Free trial
No
Free plan
No
Runs in browser
Yes
Customisable
Yes
Website
clinion.com

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Clinion FAQs

A clinical trial management system for sponsors and CROs covering Phase I to IV studies, with protocol deviation management and real-time milestone tracking.

Capturing protocol deviations, tracking them centrally and notifying the right people, so issues affecting trial integrity are addressed during the study rather than discovered at database lock.

On setup speed and ease of use. It emphasises simple configuration against platforms whose implementation cycles can run for months.

Yes. CTMS sits within an integrated suite, and deep integration across those products is a stated advantage.

Pricing is not published. Quotes reflect study volume and which suite products are licensed alongside CTMS.