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What is myoRESEARCH?

Seamlessly collect and integrate various data types all within one software solution. The synergy of electromyography, force, pressure, motion, and high-speed video is improved through automatic synchronization, leading to a smarter workflow and reliable data. The tasks of gathering, reviewing, analyzing, and reporting have been significantly streamlined, even when navigating complex biomechanics recording systems. With the myoRESEARCH® module configurations, users can effortlessly select the devices needed for their sessions, ensuring real-time automatic synchronization of data. Customize your myoRESEARCH software to fit any combination of Noraxon modules that fulfill your specific measurement needs. Additionally, we offer a complimentary analysis-only version of our software for current MR3 users. Whether you aim to enhance your understanding, hone your abilities, or analyze data outside the lab, we provide extensive support tailored to your objectives. Our dedication to improving user experience not only removes obstacles but also promotes easier access to advanced data analysis resources, making it simpler for users to engage with complex data. This commitment reflects our belief that everyone should have the opportunity to leverage sophisticated tools for their research and analysis endeavors.

What is Veeva SiteVault?

Improve the efficiency of regulatory operations within your organization to strengthen compliance and promote research progress. Veeva SiteVault streamlines the management of clinical trials by consolidating regulatory responsibilities, resulting in heightened effectiveness and adherence to necessary regulations. You can manage regulatory and source documents through a single platform that meets 21 CFR Part 11 and HIPAA requirements. With real-time data across all trials, SiteVault Enterprise enhances operational performance, speeds up study initiation, and supports rapid, high-quality trial management. Move away from manual processes and personalize your workflows to improve both quality and speed in study activation. By providing monitors with secure, direct access to your regulatory and source documents, you eliminate the complications associated with EMR access and document redaction. Additionally, you can customize your workflows, create reports, and develop dashboards that offer valuable insights into start-up timelines and regulatory processes, ultimately driving improved results for your clinical trials. This holistic strategy not only simplifies processes but also fosters greater collaboration among teams, enabling better communication and efficiency throughout the trial phases. As a result, your organization can achieve its research goals while maintaining rigorous compliance standards.

Media

Media

Integrations Supported

Kinduct
Microsoft 365

Integrations Supported

Kinduct
Microsoft 365

API Availability

Has API

API Availability

Has API

Pricing Information

Pricing not provided.
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

Noraxon USA

Date Founded

1987

Company Location

United States

Company Website

www.noraxon.com/our-products/myoresearch/

Company Facts

Organization Name

Veeva Systems

Company Location

United States

Company Website

sites.veeva.com/products/sitevault-enterprise/

Categories and Features

Scientific Data Management System (SDMS)

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

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

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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