Clinion
About Clinion
An AI-enabled eClinical platform for clinical trials. Provides a unified suite of tools including EDC, RTSM, CTMS, eConsent, ePRO, eSource, and eTMF to automate study management, data capture, and regulatory compliance.
Clinion is an AI-powered eClinical platform designed to streamline the entire clinical trial lifecycle. By unifying essential modules like EDC, RTSM, CTMS, eConsent, and ePRO into a single ecosystem, it reduces the need for disparate systems and manual data reconciliation. The platform is particularly notable for its deep integration of AI, which automates labor-intensive tasks such as protocol drafting, medical coding, and CSR generation. Designed for sponsors and CROs, Clinion supports global trials with multilingual capabilities and a BYOD-friendly ePRO application. While the platform is highly integrated, its modular nature allows it to function as a standalone solution or as part of a broader eClinical suite. Support is provided through dedicated account management and a responsive customer experience team, with documentation and demo resources available for prospective users.
Pros & Cons
- AI-driven automation significantly reduces study setup and data management timelines.
- Unified platform architecture eliminates the need for multiple system logins and manual data integration.
- Supports global trials with multilingual forms and flexible deployment options.
- Real-time data validation and automated audit trails ensure high data quality and regulatory compliance.
- BYOD-friendly ePRO application increases patient convenience and study compliance.
- Pricing is not publicly disclosed and requires a sales consultation.
- Extensive feature set may require a learning period for teams transitioning from legacy systems.
- Integration with external non-Clinion systems may require custom configuration.
Features
Key features
Automates study setup, CDASH mapping, remote source data verification, and medical coding.
Automates patient randomization, kit assignment, and supply logistics directly within the EDC.
Captures patient-reported outcomes via mobile app or web with automated reminders and real-time syncing.
Simplifies informed consent with multimedia forms, real-time tracking, and patient-friendly UX.
Unifies project tracking, site monitoring, and financial management in one integrated system.
Auto-generates ICH M11 and TransCelerate-compliant protocol drafts from study summaries.
Extracts key insights from protocols and study data to generate high-quality clinical study reports.
Additional features
Digitally manages trial documents with audit trails, bulk uploads, and DIA-based structures.
Uploads, de-identifies, and accesses medical images directly within the EDC.
Surfaces protocol insights, operational metrics, and live study data through AI-powered conversation.
Validates data entries instantly for accuracy during capture.
Logs all data changes automatically to maintain regulatory compliance.
Provides clinical teams with real-time dashboards for patient data review.
Configures patient surveys and forms in multiple languages for global trials.
Pricing
Countries & Languages
Interface languages
Billing currencies
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About Clinion
An AI-enabled eClinical platform for clinical trials. Provides a unified suite of tools including EDC, RTSM, CTMS, eConsent, ePRO, eSource, and eTMF to automate study management, data capture, and regulatory compliance.
Clinion Details
Clinion's In-App Market Place
Does Clinion have an in-app market place?
Yes
How many Mini-Apps in the marketplace?
8
Mini Apps
1. Clinion eCOA Mobile App: Allows patients to easily access and complete electronic clinical outcome assessments on their mobile devices
improving convenience and compliance.
2. Clinion eCOA Scheduler Plugin: Integrates with scheduling systems to automatically remind patients about upcoming assessments and appointments
reducing no-show rates.
3. Clinion eCOA eConsent Module: Streamlines the informed consent process by enabling patients to review and sign consent forms electronically
increasing efficiency and compliance.
4. Clinion eCOA Reporting Dashboard: Provides real-time data visualization and analytics tools to track patient progress and outcomes
making it easier for researchers to monitor study results.
Pricing Options
Accepted Payment Currencies
USD ($), EUR (โฌ), GBP (ยฃ), JPY (ยฅ), AUD (A$), CAD (C$), CHF (Fr), CNY (ยฅ), SEK (kr), SGD (S$), INR (โน), HKD (HK$), KRW (โฉ), NZD (NZ$), RUB (โฝ), ZAR (R), BRL (R$), MXN (Mex$), TRY (โบ), NOK (kr), DKK (kr), PLN (zล), THB (เธฟ), MYR (RM), IDR (Rp), TWD (NT$), PHP (โฑ).
Pros & Cons
- AI-driven automation significantly reduces study setup and data management timelines.
- Unified platform architecture eliminates the need for multiple system logins and manual data integration.
- Supports global trials with multilingual forms and flexible deployment options.
- Real-time data validation and automated audit trails ensure high data quality and regulatory compliance.
- BYOD-friendly ePRO application increases patient convenience and study compliance.
- Pricing is not publicly disclosed and requires a sales consultation.
- Extensive feature set may require a learning period for teams transitioning from legacy systems.
- Integration with external non-Clinion systems may require custom configuration.
Clinion's Support Options
Email Address
support@clinion.comContact
1-800-123-4567Documentation
https://docs.clinioneCOA.comCommunity Forums
https://community.clinioneCOA.comChatbot
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