About Clinion
Clinion by Clinion IT Services is a comprehensive clinical research software platform designed to streamline and simplify the management of clinical trials from study initiation to completion.
Clinion by Clinion IT Services is a comprehensive clinical research software platform designed to streamline and simplify the management of clinical trials from study initiation to completion. Built to support pharmaceutical companies, biotechnology firms, contract research organizations (CROs), medical device manufacturers, and research institutions, the platform integrates multiple clinical trial processes into a centralized environment. Clinion offers a suite of tools that includes Electronic Data Capture (EDC), Clinical Trial Management System (CTMS), electronic Patient Reported Outcomes (ePRO), Randomization and Trial Supply Management (RTSM), eConsent, medical coding, and reporting capabilities. By consolidating these essential functions into a unified platform, Clinion helps research organizations improve operational efficiency, enhance data quality, and maintain regulatory compliance throughout the clinical trial lifecycle.
Pros & Cons
- It slashes your overall clinical trial costs by up to 35 percent.
- It helps get medical products to market 30 percent faster than usual.
- You can get a study completely built and configured in just two weeks.
- It cuts down protocol drafting times and expenses by 60 percent.
- The platform comes fully compliant with global standards like FDA, HIPAA, and GDPR.
- You still need human experts to double-check and validate the AI-generated protocols.
- Managing eleven separate software modules could feel overwhelming for smaller operations.
- Patients are forced to use digital devices to fill out forms and give consent.
- Report accuracy relies heavily on AI perfectly extracting data from complex source documents.
- The website forces users to deal with cookie configuration settings immediately upon visiting.
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
This feature automates clinical trial phases using AI to optimize operational speed and cost efficiency.
It automatically creates compliant trial protocol drafts from study summaries within minutes on a unified platform.
It utilizes AI to instantly extract key insights from various study documents to generate high-quality clinical study reports.
This centralizes study management by tracking milestones, monitoring clinical sites, and managing budgets in one integrated system.
It automates randomization and supply logistics while offering flexibility, speed, and regulatory compliance.
This simplifies patient-reported data capture via multilingual forms, automated reminders, and seamless EDC integration.
It captures accurate source data in real-time with built-in validations and direct integration into the EDC.
It streamlines the informed consent process using interactive multimedia forms and real-time tracking.
This provides digital trial document management featuring audit trails, bulk uploads, and a prebuilt structure based on DIA.
It allows users to upload, de-identify, and access medical images through AI-powered automation inside the EDC.
This delivers protocol insights and live study metrics through a single AI-powered conversational interface.
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About Clinion
Clinion by Clinion IT Services is a comprehensive clinical research software platform designed to streamline and simplify the management of clinical trials from study initiation to completion.
Clinion Details
Clinion's In-App Market Place
Does Clinion have an in-app market place?
Yes
How many Mini-Apps in the marketplace?
1
Mini Apps
N/A
Pricing Options
Accepted Payment Currencies
USD ($), EUR (€), GBP (£), JPY (¥), AUD (A$), CAD (C$), CHF (Fr), CNY (¥), SEK (kr), SGD (S$), INR (₹), HKD (HK$), KRW (₩), NZD (NZ$), RUB (₽), ZAR (R), BRL (R$), MXN (Mex$), TRY (₺), NOK (kr), DKK (kr), PLN (zł), THB (฿), MYR (RM), IDR (Rp), TWD (NT$), PHP (₱)., USD
Pros & Cons
- It slashes your overall clinical trial costs by up to 35 percent.
- It helps get medical products to market 30 percent faster than usual.
- You can get a study completely built and configured in just two weeks.
- It cuts down protocol drafting times and expenses by 60 percent.
- The platform comes fully compliant with global standards like FDA, HIPAA, and GDPR.
- You still need human experts to double-check and validate the AI-generated protocols.
- Managing eleven separate software modules could feel overwhelming for smaller operations.
- Patients are forced to use digital devices to fill out forms and give consent.
- Report accuracy relies heavily on AI perfectly extracting data from complex source documents.
- The website forces users to deal with cookie configuration settings immediately upon visiting.
Clinion's Support Options
Email Address
support@clinion.comChatbot
Available