AI TOOL PROFILE
Clinion: AI-Powered eClinical Platform for Clinical Trials
- Healthcare
- Clinical Trial Management
- Pharmaceutical companies
- Clinical Research Organizations (CROs)
- Healthcare companies managing clinical trials
Pricing
Clinion offers a free product option. Pricing for other tiers was not clearly available from the provided evidence; buyers should confirm current pricing on the vendor website.
At a glance
- Best for
- Pharmaceutical companies, Clinical Research Organizations (CROs), Healthcare companies managing clinical trials
- Key use cases
- Clinical Study Setup, Patient Data Management, Regulatory Reporting, Trial Logistics
- Official website
- Visit clinion official website
How AI is used
Clinion is an eClinical platform designed for healthcare and pharmaceutical companies, as well as Clinical Research Organizations (CROs). It provides integrated tools to manage various stages of a clinical trial, including study setup, data collection, and reporting.
The software includes modules such as Electronic Data Capture (EDC), a Clinical Trial Management System (CTMS), and tools for electronic consent and patient-reported outcomes. AI is used to support medical coding, protocol drafting, and populating clinical study reports.
Buyers should confirm how AI-generated drafts align with their specific regulatory requirements and whether the unified suite meets all their operational needs.
Compliance certifications include SOC 2 Type II, ISO 27001, ISO 9001, ISO 42001, GDPR, and HIPAA.
Key Features
AI-driven EDC
Electronic Data Capture that supports medical coding, data review, and study setup.
eProtocol Automation
AI that helps generate ICH M11 and TranCelerate-compliant protocol drafts from study summaries.
CSR Automation
Extracts insights from protocols, SAP, and TLFs to auto-populate parts of Clinical Study Reports.
Centralized CTMS
A system for tracking project milestones, monitoring sites, and managing budgets.
RTSM
Automates patient randomization and supply logistics, integrated within the EDC.
eConsent and ePRO
Digital tools for managing informed consent and capturing patient-reported outcome data.
eTMF
Electronic Trial Master File for managing trial documents with audit trails and DIA-based structures.
Use Cases
Clinical Study Setup
Using AI to help create initial protocol drafts and configure EDC settings.
Patient Data Management
Capturing source data in real time and recording patient-reported outcomes via eSource and ePRO.
Regulatory Reporting
Supporting the generation of Clinical Study Reports by extracting data and insights through AI.
Trial Logistics
Managing patient randomization and kit assignments through the integrated RTSM tool.
FAQ
What is Clinion used for?
- Clinion is used to manage clinical trials through a unified suite of tools including Electronic Data Capture (EDC), CTMS, eConsent, and AI-driven protocol and report generation.
Is Clinion compliant with healthcare data standards?
- The platform is designed to be compliant with HIPAA, GDPR, SOC 2 Type II, and various ISO standards including ISO 27001.
How does AI help in the Clinion platform?
- Clinion uses AI to help auto-generate protocol drafts, perform medical coding and data review in the EDC, and auto-populate parts of Clinical Study Reports (CSRs).
Does Clinion offer a free version?
- The provided evidence indicates that Clinion offers a free product option.
Source category: Healthcare
Source subcategory: Clinical Trial Management
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