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What is studioMED+?

Germany stands at the forefront of research in Europe, undertaking more than 600 clinical and non-clinical studies annually. The complexity of managing these studies is increasing, necessitating meticulous coordination of appointments and personnel, prompt updates of study data, and straightforward access to documents for inquiries. It's essential to move away from the constraints of a paper-based system; by opting for a lightweight tablet, you can access information in seconds, allowing you to focus on what truly drives progress in your research. The digital study management solution offered by studioMED+ is crafted to assist you in making this vital transition. No matter where you are or what time it is, studioMED+ provides a flexible tool that effortlessly adapts to your unique requirements, ensuring your research process remains both efficient and effective. By embracing this innovative solution, you will not only enhance your productivity but also position yourself at the cutting edge of study management advancements. Make the switch today and witness how streamlined processes can transform your research endeavors.

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.

Media

Media

Integrations Supported

Additional information not provided

Integrations Supported

Additional information not provided

API Availability

Has API

API Availability

Has API

Pricing Information

$200 per month
Free Trial Offered?
Free Version

Pricing Information

Pricing not provided.
Free Trial Offered?
Free Version

Supported Platforms

SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux

Supported Platforms

SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Company Facts

Organization Name

studio.201 software

Date Founded

2019

Company Location

Germany

Company Website

www.studiomedplus.de

Company Facts

Organization Name

QMENTA

Company Location

Spain

Company Website

www.qmenta.com

Categories and Features

Clinical Trial Management

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

Categories and Features

Clinical Trial Management

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

Medical Imaging

Automated Routing
Comparison View
Compliance Management
Data Import / Export
Diagnostic Reporting
Image Analytics
Treatment Planning
Workflow Management

Radiology

Audit Trail
Billing & Invoicing
Claims Management
EDI
EMR HL7 Bridge
Image Fusion
PACS Integration
Patient Scheduling
Scanning Input
Teleradiology
Wait List Management

Scientific Data Management System (SDMS)

Analytics
Artificial Intelligence (AI)
Audit
Centralized Data Repository
Collaboration
Compliance
Data Security
ELN Integration
LIMS Integration
Workflows

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