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What is QMENTA?

An advanced cloud platform that can be accessed globally, infinitely adaptable, and driven by artificial intelligence offers collaborative functionalities while maintaining the highest levels of security and compliance. Created by experts in neuroimaging and data science, this intuitive software meets the intricate and specialized needs of the neuroscience sector. Tailored to match your unique requirements, it accommodates a variety of tasks, such as research, clinical trials, point-of-care applications, algorithm creation, and the analysis of brain-related data. The platform enables worldwide data aggregation and consolidates imaging studies within a unified cloud framework. It serves as an effective, all-encompassing management solution for both clinical and real-world data, as well as medical imaging information. Users benefit from personalized expert support throughout their projects, ensuring the achievement of favorable results. Additionally, it incorporates centralized reading features and allows for the comparison of quantitative findings with a normative database. The platform guarantees high-quality, shareable reports and data export options that simplify the submission approval process, making it an indispensable resource for professionals in neuroscience. Moreover, its cutting-edge design promotes collaboration among researchers and clinicians, cultivating a vibrant community committed to pushing the boundaries of the field. With these capabilities, the platform stands out as a transformative tool that not only enhances individual research but also drives collective advancements in neuroscience.

What is EvidentIQ?

EvidentIQ's eCOA simplifies the process of gathering real-time data directly from patients via an intuitive interface, which not only improves patient evaluations but also elevates the quality of data collected. Clients can opt for a comprehensive eCOA package or customize their selection by combining different components to meet specific requirements. By arranging a demonstration with our expert team, you can learn how to optimize the return on investment for your research initiatives. The eCOA platform integrates data science services with advanced technology, offering a flexible solution. It functions independently of specific eClinical technologies such as EDC systems, while also providing smooth integration with current eClinical software environments. This system is designed to efficiently collect a diverse array of outcome data from patients, healthcare professionals, or observers, ensuring compliance and improving the data collection experience overall. With its adaptable nature, organizations can tailor the eCOA framework for various clinical trial situations, thereby significantly enhancing their research capabilities and outcomes. Such customization not only meets immediate needs but also prepares teams for future challenges in clinical research.

Media

Media

Integrations Supported

Additional information not provided

Integrations Supported

Additional information not provided

API Availability

API Availability

Pricing Information

Pricing not provided

Pricing Information

Pricing not provided
Free Trial Offered?

Supported Platforms

SaaS

Supported Platforms

SaaS

Customer Service / Support

Web-Based Support

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Training Options

Documentation Hub
Webinars
Online Training

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Company Facts

Organization Name

QMENTA

Company Location

Spain

Company Website

www.qmenta.com

Company Facts

Organization Name

EvidentIQ

Company Location

Germany

Company Website

www.evidentiq.com

Categories and Features

Clinical Trial Management

21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
HIPAA Compliant

Medical Imaging

Comparison View
Compliance Management
Data Import / Export
Image Analytics
Treatment Planning
Workflow Management

Radiology

Audit Trail
Image Fusion
PACS Integration

Categories and Features

Clinical Trial Management

21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
HIPAA Compliant
Patient Database
Recruiting Management
Scheduling

Electronic Data Capture

Audit Trail
CRF Tracking
Data Verification
Distributed Capture
Forms Management
Remote Capture

Patient Experience

Not specified

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