Clinion: AI-Powered eClinical Platform for Clinical Trials
Clinion helps sponsors and CROs manage clinical trials. It is designed for organizations that need a unified suite for data capture, patient consent, and regulatory reporting.
At a glance
- Category
- Healthcare
- Best for
- 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.
- Key use cases
- Clinical Study Setup, Patient Data Management, Regulatory Reporting, Trial Logistics
- Official website
- clinion.ai
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
Electronic Data Capture that supports medical coding, data review, and study setup.
AI that helps generate ICH M11 and TranCelerate-compliant protocol drafts from study summaries.
Extracts insights from protocols, SAP, and TLFs to auto-populate parts of Clinical Study Reports.
A system for tracking project milestones, monitoring sites, and managing budgets.
Automates patient randomization and supply logistics, integrated within the EDC.
Digital tools for managing informed consent and capturing patient-reported outcome data.
Electronic Trial Master File for managing trial documents with audit trails and DIA-based structures.
Use Cases
Using AI to help create initial protocol drafts and configure EDC settings.
Capturing source data in real time and recording patient-reported outcomes via eSource and ePRO.
Supporting the generation of Clinical Study Reports by extracting data and insights through AI.
Managing patient randomization and kit assignments through the integrated RTSM tool.
Best For
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.
FAQ
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.
The platform is designed to be compliant with HIPAA, GDPR, SOC 2 Type II, and various ISO standards including ISO 27001.
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).
The provided evidence indicates that Clinion offers a free product option.
Source category: Healthcare
Source subcategory: Clinical Trial Management
