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features
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support

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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

Protocol Manager is instrumental for clinical operations in overseeing global trials across various phases of drug, device, biologic, and vaccine development. By implementing the necessary Standard Operating Procedures (SOPs), Protocol Manager ensures compliance with the FDA’s 21 CFR part 11 regulations. The platform utilizes Web Services technology to facilitate effortless and automatic integration with numerous widely-used EDC and IVRS solutions. For those systems that lack Web Services compatibility, an export/import mechanism is available for integration. This comprehensive tool features a powerful tracking system and database that effectively manages a wide range of trial information and metrics, enhancing overall operational efficiency. Additionally, it empowers organizations to maintain rigorous oversight throughout the trial process, ensuring data integrity and compliance at every stage.

API Access

Has API No 

API Access

Has API No 

Screenshots View All

Screenshots View All

Integrations

EDGE Yes 

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 Yes 

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 Yes 
Mac Yes 
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) No 
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 No 

Vendor Details

Company Name

AQ Trials

Founded

2017

Country

United Kingdom

Website

aq-trials.com

Vendor Details

Company Name

Atlant Systems

Founded

2010

Country

United States

Website

atlantsystems.com

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 Yes 
Document Management Yes 
Electronic Data Capture No 
Enrollment Management No 
HIPAA Compliant Yes 
Monitoring Yes 
Patient Database Yes 
Recruiting Management No 
Scheduling Yes 
Study Planning Yes 

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