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Ratings and Reviews 0 Ratings
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What is nQuery?
Discover the numerous benefits of nQuery, which range from conducting sample size and power analyses to facilitating cutting-edge adaptive trial designs, thus positioning itself as the premier platform for trial design that not only expedites clinical studies but also minimizes costs while improving success rates. Researchers and biostatisticians around the world favor nQuery as a solution to the increasing intricacies of clinical trials, surging expenses, and changing regulations. Its user-friendly, spreadsheet-like interface allows for quick calculations of sample sizes suitable for FDA and EMA submissions without the need for any coding expertise. Serving both Frequentist and Fixed-term trials, nQuery simplifies reporting for all parties involved in the trial process. Users can benefit from realistic predictions of expected timelines and expenses, ensuring that their sample sizes are in harmony with both scientific insights and budgetary constraints. Additionally, nQuery's multiple factors tool enables precise adjustments to calculations, boasting over 1000 methods for sample size and power calculations, which allows for rapid determination of sample sizes in various contexts. By leveraging nQuery’s extensive features, you can confidently navigate the complexities of contemporary clinical trials and enhance the efficiency of your research endeavors. Embracing nQuery means embracing a smarter, more effective way to conduct clinical research in an ever-evolving landscape.
What is Transition Technologies eCRF?
Our adaptable electronic Case Report Form (eCRF) platform is specifically crafted for non-commercial clinical trials and can easily be customized to align with any study protocol.
Created through years of close collaboration with medical professionals and researchers, our eCRF solution emphasizes user-friendliness, featuring an intuitive and flexible interface.
Moreover, the system adheres to all required quality standards, and because we have full control over the code, we can continuously improve and adjust it to meet changing regulatory requirements and the evolving nature of clinical trials.
This commitment ensures that our platform remains not only relevant but also at the forefront of innovation, effectively addressing the needs and expectations of both researchers and participants.
Ultimately, this proactive approach fosters a reliable environment for conducting clinical trials, enhancing the overall quality of research outcomes.
Media
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Integrations Supported
Additional information not provided
Integrations Supported
Additional information not provided
API Availability
Has API
API Availability
Has API
Pricing Information
Pricing not provided.
Free Trial Offered?
Free Version
Pricing Information
$45k licence
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
Statistical Solutions
Company Location
United States
Company Website
www.statsols.com
Company Facts
Organization Name
Transition Technologies Science Sp. z o.o.
Date Founded
2020
Company Location
Poland
Company Website
www.ecrf.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
