Fusion eClinical Suite logo

Fusion eClinical Suite

by Axiom Real-Time Metrics · Since 2000
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ActiveAvailable globallyCloud
Quick facts
VendorAxiom Real-Time Metrics
Year launched2000
StatusActive
Location5520 Explorer Dr, 4th Floor Mississauga, ON L4W 5L1, Canada
Countries servedGlobal
Languages1
Integrations
Free tier
Free trial
Contact salesYES

About Fusion eClinical Suite

Fusion eClinical Suite is a clinical trial management software from Axiom Real-Time Metrics that supports the management of clinical trials. It combines data collection, reporting, and integration with third-party systems so users can simplify their clinical research processes. The platform allows for real-time data monitoring and analysis, which facilitates timely decision-making in clinical studies. Fusion eClinical Suite is designed to improve collaboration among research teams while ensuring compliance with regulatory standards. Key capabilities: data collection real-time reporting integration with third-party systems user-friendly dashboard compliance tracking Best for: clinical research organizations that need to manage and analyze data across multiple clinical trials.

Fusion eClinical Suite is a comprehensive software solution designed for Clinical Trial Management and Electronic Data Capture. This powerful tool stands out for its ability to streamline the process of collecting, managing, and analyzing data in clinical trials, ultimately helping research teams save time and improve efficiency. The user interface of Fusion eClinical Suite is intuitive and user-friendly, making it easy for both experienced researchers and newcomers to navigate the system. The design is clean and organized, with a focus on simplicity that enhances the overall user experience. The platform offers customization options, allowing users to tailor their workspace to suit their individual preferences. What sets Fusion eClinical Suite apart from its competitors is its innovative features, such as real-time data capture and monitoring capabilities. This allows research teams to track and analyze data as it is collected, enabling them to make timely decisions and adjustments during the trial process. The software also offers advanced reporting tools that provide in-depth insights into trial progress and outcomes.

Pros & Cons

What users like
  • +Comprehensive Solution: Offers a wide range of integrated modules for various clinical trial needs.
  • +User-Friendly Interface: Designed for ease of use, even for those with limited technical expertise.
  • +Real-Time Data Access: Provides immediate access to study data, facilitating timely decision-making.
  • +Regulatory Compliance: Supports adherence to industry standards and regulations.
What users flag
  • Pricing Transparency: Lack of publicly available pricing information may require direct contact for quotes.
  • Learning Curve: Some users may experience a learning curve due to the platform's extensive features.
  • Limited Language Support: Currently available only in English.
  • No In-App Marketplace: Absence of an in-app marketplace for additional features or services

Features

Key features

Electronic Data Capture (EDC)
Facilitates real-time data collection and management.
Data Management (DM)
Centralizes and streamlines data handling processes.
Randomization and Trial Supply Management (RTSM)
Manages subject randomization and clinical trial supplies.
Clinical Trial Management System (CTMS)
Oversees and monitors clinical trial progress.
Inventory Management
Tracks and manages clinical trial inventory.
Electronic Patient-Reported Outcomes (ePRO)
Collects patient-reported data electronically.
Electronic Consent (eConsent)
Manages electronic consent processes.
Adverse Event/Serious Adverse Event (AE/SAE) Tracking
Monitors and reports adverse events.
Safety Database
Manages pharmacovigilance data.
Clinical Trial Management System (CTMS) Reporting
Provides comprehensive reporting capabilities.
Deviation Tracking
Identifies and manages study deviations.
Payment Tracking
Manages and tracks study-related payments.
Monitor Trip Reporting
Tracks and reports on monitoring trips.
Electronic Trial Master File (eTMF)
Manages trial documentation electronically.
Central/Local Lab Import
Integrates laboratory data into the system.
Adjudication
Manages and tracks adjudication processes.
Imaging
Manages and integrates imaging data.

Additional features

Electronic Data Capture (EDC)
Facilitates real-time data collection and management.
Data Management (DM)
Centralizes and streamlines data handling processes.
Randomization and Trial Supply Management (RTSM)
Manages subject randomization and clinical trial supplies.
Clinical Trial Management System (CTMS)
Oversees and monitors clinical trial progress.
Inventory Management
Tracks and manages clinical trial inventory.
Electronic Patient-Reported Outcomes (ePRO)
Collects patient-reported data electronically.
Electronic Consent (eConsent)
Manages electronic consent processes.
Adverse Event/Serious Adverse Event (AE/SAE) Tracking
Monitors and reports adverse events.
Safety Database
Manages pharmacovigilance data.
Clinical Trial Management System (CTMS) Reporting
Provides comprehensive reporting capabilities.
Deviation Tracking
Identifies and manages study deviations.
Payment Tracking
Manages and tracks study-related payments.
Monitor Trip Reporting
Tracks and reports on monitoring trips.
Electronic Trial Master File (eTMF)
Manages trial documentation electronically.
Central/Local Lab Import
Integrates laboratory data into the system.
Adjudication
Manages and tracks adjudication processes.
Imaging
Manages and integrates imaging data.

Pricing

Free trial
Free version
Request a quote
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Countries & Languages

Global
Countries served
1
Interface languages
15
Billing currencies

Interface languages

English

Billing currencies

🇺🇸USD🇪🇺EUR🇬🇧GBP🇯🇵JPY🇦🇺AUD🇨🇦CAD🇨🇭CHF🇨🇳CNY🇸🇪SEK🇲🇽MXN🇮🇳INR🇧🇷BRL🇭🇰HKD🇸🇬SGD🇿🇦ZAR

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