End-to-End Connected Clinical Research Platform
Modern clinical research platform built for regulated oversight and unified control across study operations, documentation, and quality processes within one connected system.
20+
Clinical research expertise
GCP · UK GDPR · 21 CFR Part 11
Regulatory alignment
7 Connected Modules
One controlled environment
NHS · CROs · Sponsors · Academic
Built for all environments
Built by people who have worked in clinical research.
AQ Trials is built by clinicians and research professionals with over 20 years of experience across healthcare and regulated clinical research environments.
AQ unifies CTMS, eTMF, eISF, ePSF, QMS, and CAPA within one controlled system — and continues to evolve alongside advancing regulatory expectations and multi-study complexity.
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20+
years of experience in clinical research and regulated environments
Founded by clinicians and research professionals
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See AQ in action.
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team.
Why we built AQ?
AQ was built to establish a connected research environment where every function operates within one controlled structure.
Clinical research operations require coordination across study activity, documentation, quality oversight, and pharmacy accountability within regulated environments.
Align study operations, documentation, and quality processes within one system.
Establish clear ownership and traceable activity across teams.
Maintain continuous inspection readiness without manual reconstruction.
Support controlled execution across multi-study clinical programmes.
Who AQ is for
AQ supports organisations operating across regulated clinical research environments where structured oversight, audit traceability, and coordinated execution remain essential.
Contract Research Organisations (CROs)
Manage multi-study portfolios, sponsor deliverables, and cross-site coordination with consistent operational visibility and quality governance.
Sponsors and Biopharmaceutical Companies
Maintain oversight across study execution, site performance, documentation completeness, and CAPA processes throughout clinical programmes.
Hospitals and NHS Research Sites
Coordinate clinical workload alongside research governance with structured documentation control, participant tracking, and inspection-ready oversight.
Academic and University Research Institutions
Manage investigator-led and collaborative studies with controlled documentation, study coordination, and regulatory compliance across research portfolios.
What AQ helps solve.
AQ addresses the operational pressure points that research teams manage across regulated clinical environments.
PROBLEM
Fragmented Study Systems
Structured in one controlled environment
AQ unifies CTMS, eTMF, eISF, ePSF, QMS, and CAPA so study operations, documentation, and quality processes remain linked.
PROBLEM
Limited Operational Visibility
Real-Time Study Oversight
AQ provides a clear view across participant activity, documentation status, quality events, and pharmacy records.
PROBLEM
Manual Coordination Across Teams
Structured Workflow Control
AQ aligns investigators, coordinators, quality teams, and pharmacy staff within defined workflows.
PROBLEM
Audit Preparation Pressure
Continuous Inspection Readiness
AQ maintains time-stamped records, document version control, and traceable actions so study history remains organised.
PROBLEM
Inconsistent Quality & CAPA Tracking
Integrated Governance
AQ connects deviation management, incident tracking, and CAPA workflows directly with study execution.
PROBLEM
Scaling Across Multiple Studies
Controlled Multi-Study Execution
AQ supports structured study environments with consistent processes for expanding research portfolios.
Continuously Evolving with Clinical Research
Clinical research continues to advance with increasing regulatory expectations, multi-study complexity, and expanding data requirements. AQ evolves alongside this environment, strengthening connected oversight, structured governance, and operational clarity across clinical programmes.
Regulatory Alignment and Compliance Standards
Continuous alignment with GCP, UK GDPR, Data Protection Act 2018, and 21 CFR Part 11 to support audit-ready research environments.
AI-Assisted Operational Intelligence
Enhancements in document intelligence, readiness monitoring, workflow guidance, and early quality signal detection across studies.
Scalable Multi-Study Architecture
Ongoing optimisation to support expanding research portfolios, multi-site coordination, and structured study environments.
Interoperability and System Connectivity
Integration capabilities with external research systems including EDC, IWRS, and other clinical data platforms.
User-Centric Workflow Improvements
Continuous refinement of workflows, role-based access, and usability aligned with real research team operations.
Security, Data Integrity, and Audit Traceability
Strengthening data protection, version control, and time-stamped audit logs across all modules and study activities.
Here is what our Clients are saying About us
It was a very good experience
This has revolutionised the way we work and improved efficiencies and study compliance reducing admin time spent sending reminders.
– Angie H.
Research Nurse
Both the AQ product and the team were flexible in their approach, they listened to our challenges and were able to embed the AQ platform with ease. The team was trained quickly and we were up and running in no time. The system has enabled us to manage more studies and transformed the way we work.
It was a very good experience
– Fran Westwell
Lead / Senior Research Nurse
It was a very good experience
The AscensionQ platform has helped my research staff set-up multiple studies faster and manage participant appointments more effectively. The software is easy to use and the team is always there to help us.
– Fran Westwell
Lead / Senior Research Nurse
Request a live demo to understand AQ's direction.
See how AQ brings study operations, documentation, and quality governance into one connected, controlled environment. Explore how research teams gain structured oversight, operational visibility, and continuous inspection readiness.
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