Average Ratings 0 Ratings
Average Ratings 0 Ratings
Description
AQ Platform is an advanced software solution tailored for managing clinical research across NHS trusts, clinical trial units, investigator sites, site networks, CROs, sponsors, and academic research groups. It comprises various modules that facilitate trial management, electronic documentation for trials and investigator sites, pharmacy and laboratory operations, quality assurance, corrective and preventive actions (CAPA), and the digital delegation of authority. The platform enables seamless integration of controlled trial records and comprehensive audit trails for efficient study operations. Utilizing Connected Intelligence, the software employs AI to identify potential gaps and suggest subsequent actions, with each recommendation requiring validation from a designated user, ensuring that customer data remains confidential and is not utilized for AI model training. Deployed within Microsoft Azure's UK regions, AQ Platform is meticulously designed to align with ICH E6(R3) and the standards expected by the MHRA for Good Clinical Practice inspections. Additionally, AQ Trials has achieved NHS DSPT Standards Met (2026) and holds Cyber Essentials certification, reflecting its commitment to security and regulatory compliance. Developed by Phase 1 trial physicians, the system allows for the individual deployment of its modules, and it has been actively utilized in NHS operations since 2020, demonstrating its effectiveness and reliability in real-world clinical settings. With ongoing enhancements and user feedback, the platform continues to evolve, ensuring it meets the changing needs of clinical research.
Description
Experience the forefront of eSource, CTMS, and eRegulatory software designed specifically for clinical trial sites. With CRIO’s top-tier electronic source, you can effortlessly capture source data in real-time, drastically cutting down on paper usage by up to 90% while enhancing data quality by 80%. Gain command over your operations through CRIO’s user-friendly Clinical Trial Management System, allowing you to efficiently schedule patients, monitor financials, and optimize recruiting processes. We proudly present cutting-edge electronic regulatory binders, including the innovative first-ever electronic delegation log, all compliant with 21 CFR Part 11 standards. For clinical trial sponsors, you can perform 100% remote monitoring of your sites’ source data and regulatory documents through a secure online portal. Become a part of our extensive network of over 500 clinical research sites worldwide. Our commitment is to facilitate the growth of your business by streamlining your site’s operations, ensuring that your studies can continue smoothly, regardless of whether you're on-site or not. This way, you can focus on what truly matters: advancing your clinical research initiatives.
API Access
Has API
No
API Access
Has API
No
Integrations
EDGE
No
Pricing Details
Pricing is modular and quoted for each organization based on selected modules, number of studies, and operational scale. Modules can be purchased and deployed independently; contract terms are agreed as part of the quote.
Free Trial
No
Free Version
No
Pricing Details
No price information available.
Free Trial
No
Free Version
No
Deployment
Web-Based
Yes
On-Premises
No
iPhone App
No
iPad App
No
Android App
No
Windows
No
Mac
No
Linux
No
Chromebook
No
Deployment
Web-Based
Yes
On-Premises
No
iPhone App
No
iPad App
No
Android App
No
Windows
No
Mac
No
Linux
No
Chromebook
No
Customer Support
Business Hours
No
Live Rep (24/7)
No
Online Support
Yes
Customer Support
Business Hours
Yes
Live Rep (24/7)
Yes
Online Support
Yes
Types of Training
Training Docs
Yes
Webinars
No
Live Training (Online)
Yes
In Person
No
Types of Training
Training Docs
Yes
Webinars
No
Live Training (Online)
Yes
In Person
Yes
Vendor Details
Company Name
AQ Trials
Founded
2017
Country
United Kingdom
Website
aq-trials.com
Vendor Details
Company Name
Clinical Research IO
Founded
2015
Country
United States
Website
www.clinicalresearch.io
Product Features
Clinical Trial Management
21 CFR Part 11 Compliance
No
Document Management
No
Electronic Data Capture
No
Enrollment Management
No
HIPAA Compliant
No
Monitoring
No
Patient Database
No
Recruiting Management
No
Scheduling
No
Study Planning
No
Product Features
Clinical Trial Management
21 CFR Part 11 Compliance
No
Document Management
No
Electronic Data Capture
No
Enrollment Management
No
HIPAA Compliant
No
Monitoring
No
Patient Database
Yes
Recruiting Management
No
Scheduling
Yes
Study Planning
Yes