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
Prefer a live session tailored to your team? Request a personalised demo →
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 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.
Let’s Be Clear: 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.
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.
