Ratings and Reviews 0 Ratings
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 TrialPoint?
TrialPoint™ electronic data capture (EDC) system stands out for its exceptional adaptability and ease of use, earning the trust of coordinators across the board. Our expert data managers are dedicated to converting clinical protocols into user-friendly metadata dictionaries, ensuring that TrialPoint™ is customized to meet your specific needs instead of complicating your workflows. The platform is designed to support any randomization string, media uploads, or coding dictionaries, and it includes features that allow for the concealment of treatment assignments from users. To promote efficient data collection, the system intelligently identifies visit windows and sends out alerts and reminders, which aids in keeping the whole team synchronized and focused. In today’s environment, integrating patient-reported health outcomes and quality of life assessments into clinical trials has become standard, often resulting in challenges with protocol adherence. Discover the ePRO module offered by TrialPoint, which can be tailored to fit any quality of life questionnaire or patient diary, ensuring a smooth experience for participants. This remarkable flexibility not only boosts compliance but also improves the overall integrity and quality of the data gathered in clinical research. By utilizing TrialPoint™, you can streamline your trial processes and enhance participant engagement significantly.
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
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
Statistical Solutions
Company Location
United States
Company Website
www.statsols.com
Company Facts
Organization Name
Databean
Date Founded
2007
Company Location
United States
Company Website
databean.com/trialpoint/
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