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 Biorce Aika?
Biorce's Aika is an innovative AI-powered clinical intelligence platform that revolutionizes the clinical trial lifecycle by converting labor-intensive processes for protocol creation and feasibility assessments into streamlined, evidence-based automation. Drawing on insights from nearly one million real-world trials, Aika can rapidly generate initial study protocols, detailed regulatory documents, site feasibility assessments, risk management plans, and other essential components of trials much quicker than traditional methods, thus reducing the likelihood of delays and costly revisions. This platform promotes complete transparency in its recommendation processes, empowering teams to confidently convey their decisions to regulatory bodies while ensuring expert supervision remains intact. Furthermore, Aika effectively marries the rapid efficiency of AI with deep clinical expertise, significantly shortening trial preparation durations from weeks to just days, which minimizes amendment risks and overall project vulnerabilities. By integrating seamlessly into current workflows without necessitating extensive retraining, Aika allows clinical trial teams to prioritize strategic decision-making over tedious administrative responsibilities. As a result, the focus shifts towards enhancing trial outcomes and optimizing resource allocation, ultimately driving innovation in clinical research practices.
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
Biorce
Date Founded
2024
Company Location
Spain
Company Website
www.biorce.com/our-software
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