Your team manages systems not meant to connect. There’s a better way.
The AQ walkthrough shows research teams what a single connected environment looks like across study coordination, TMF filing, site documentation, delegation records, quality oversight, and pharmacy accountability. Every session is built around your operational priorities, not a generic feature tour.
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Practical walkthroughs aligned with active research delivery.
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WATCH THE AQ PLATFORM IN ACTION
A guided walkthrough across connected AQ modules, operational workflows, and day to day clinical research activity inside the platform
What the Walkthrough Covers
A session built around your context.
The walkthrough is structured around the workflows where your team has the most friction. Whether that is study startup and TMF governance, delegation and training record management, quality oversight, or pharmacy accountability, the session starts with your priorities
Explains how connected modules change what is possible
See how CTMS, eTMF, eISF, ePSF, QMS, CAPA, and DOA operate as a single environment rather than separate tools, and what that means for audit trails, inspection readiness, and the administrative overhead your team currently carries.
Guides on where to start and how other teams have sequenced it
We cover which modules fit your immediate priorities and how organisations similar to yours have approached implementation, starting with the most urgent workflow, maintaining continuity across existing studies, and expanding as the team is ready.
Ready?
EXPLORE WHAT EACH AQ CLINICAL RESEARCH SOFTWARE MODULE OFFERS
Every AQ walkthrough includes module level workflows, operational structure, connected oversight, and platform functionality across regulated clinical research operations.
Clinical Trial Management System (CTMS)
Gives ClinOps teams and site operations a single view of study activity, visit schedules, milestone tracking, site activation status, and participant progress without toggling between spreadsheets, sponsor portals, and email threads.
Electronic Trial Master File (eTMF)
Keeps your TMF inspection ready from study start, not from the week before an audit. Controlled filing, completeness tracking, and full audit visibility across expected study documentation.
Electronic Investigator Site File (eISF)
Delegation logs, training records, investigator documentation, signatures, and site files maintained in one connected environment with attributable audit visibility.
Corrective & Preventive Action (CAPA)
Deviation reporting, root cause analysis, corrective actions, preventive actions, assigned ownership, and effectiveness review tracking with full accountability visibility.
Quality Management System (eQMS)
SOP version control, training sign off, controlled documentation, and change management maintained within one quality oversight environment.
Electronic Pharmacy Site File (ePSF)
IP accountability, dispensing records, temperature logs, and pharmacy documentation connected directly to wider study oversight workflows.
Delegation of Authority (DOA)
Delegation records, responsibility tracking, electronic signatures, and timestamped audit trails maintained across active study teams.
We are not Pushing you toward another Platform Just to add more software
AQ walkthroughs focus on helping research organisations understand where current workflows create operational pressure, fragmented oversight, duplicate administration, and accountability gaps across active studies. If AQ fits your environment, the walkthrough helps determine the right modules, rollout approach, and operational starting point.
NEED AN EVEN CLOSER LOOK AT THE AQ PLATFORM?
Book a walkthrough built around your research environment.
What UK Clinical Research Teams Say About AQ Platform?
The platform itself is simple to use, easy to administer and has a range of different functions that help to manage patients, studies, finances and analytics to interrogate the data collected across those functions. Ascension Q is more than a great platform, the team are passionate about making research easier for researchers.
– Lisa Cheng
Head of R&D
AQ is more than a great platform for the operational management and analytics of clinical trials, it’s about a team that are passionate about making a product that genuinely helps. The platform continues to grow and expand into areas of need; the developers are truly responsive. The support from the team has been exceptional.
– Rachel Thompson
Programme Manager
Very positive, easy to train new staff to use. We have been using it in our department for over 5 years now. The booking system with calendar views makes it easy to manage our very busy research clinic. The automated emails and text appointment reminders have improved compliance.
– Madi F.
Senior Research Nurse
AscensionQ has made the booking of research trial participants straightforward and efficient for our busy clinic. The reminder setup and mobile app has improved appointment compliance across all of our studies.
– Madi Farrar
Senior Research Nurse
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.
