AQ brings CTMS, eTMF, eISF, ePSF, eQMS, CAPA, and Digital DoA clinical research software modules together inside one connected platform.
trial management system providing operational oversight across study setup, participant activity, scheduling, and financial tracking.
Centralised electronic trial master file oversight with structured filing, document completeness tracking, and real-time visibility across study documentation.
Electronic Investigator Site File for structured site documentation, delegation records, and inspection-ready investigator oversight.
Electronic Pharmacy Site File supporting controlled pharmacy documentation, accountability records, and inspection-ready drug management.
Quality Management System governing policies, SOPs, document control, change management, and organisational research governance.
Corrective and Preventive Action management for deviations, incident tracking, root cause analysis, and structured resolution workflows.
Digital Delegation of Authority management for structured role assignment, signature workflows, and inspection-ready delegation.
Take a free tour of our platform features
AQ helps NHS Trust R&D departments, Clinical Research Facilities, and hospital research units bring site documentation,
AQ helps mid-market biotech and emerging sponsors maintain oversight across CROs, sites, and vendors — without building a Veeva-scale infrastructure
AQ helps academic research institutions bring consistency to clinical studies that span investigators, departments, and study types.
AQ helps CROs manage clinical trial execution across multiple sponsors, multiple studies, and multiple sites — without the data architecture compromises
AQ was built to establish a connected research environment where every function operates within one controlled structure.
Practical guides, clinical research best practices, platform updates, and industry insights — written for the people running research every day.
AQ QMS provides the core controls required to manage document governance, QCvworkflows, training requirements, competency validation, staff compliance monitoring,vand corrective resolution
Find answers to common questions, guides, troubleshooting resources, and support information to help you get the most out of our services.
verification
No spam. Unsubscribe at any time.
