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features
design
support

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Write a Review

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

Zelta is a cloud-powered platform for unified clinical data management and acquisition, designed to streamline and enhance clinical trial processes. Its modular architecture adapts to the unique demands of each study, enabling faster and more efficient outcomes. With capabilities such as electronic data capture, clinical operations management—including randomization and trial supply tracking—clinical trial management, and electronic trial master file functionality, Zelta supports comprehensive study oversight. It also enhances patient and provider engagement with electronic clinical outcome assessments and e-consent solutions. Built for studies across all phases, therapeutic areas, and global regions, Zelta offers an intuitive user experience with secure single sign-on access from anywhere. Its flexible and scalable design allows for seamless customization and integration with both native and third-party technologies, ensuring adaptability to diverse research needs.

API Access

Has API No 

API Access

Has API No 

Screenshots View All

Screenshots View All

Integrations

ClinVigilant No 
EDGE Yes 
IBM Datacap No 

Integrations

ClinVigilant Yes 
EDGE No 
IBM Datacap Yes 

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) 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 Yes 
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

Merative

Founded

2022

Country

United States

Website

www.merative.com/clinical-development

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 Yes 
Enrollment Management Yes 
HIPAA Compliant Yes 
Monitoring Yes 
Patient Database No 
Recruiting Management Yes 
Scheduling Yes 
Study Planning Yes 

Electronic Data Capture

Audit Trail Yes 
CRF Tracking Yes 
Data Entry Yes 
Data Verification Yes 
Distributed Capture Yes 
Document Imaging Yes 
Document Indexing Yes 
Forms Management Yes 
Remote Capture Yes 
Study Management Yes 

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