Reset how you manage your clinical trial workflow
Best-in-class clinical trial management systems
Clinibase builds tailored end-to-end trial recruitment workflow solutions that support CROs and sponsor organisations like yours, to take the pain out of reporting, billing, and recruiting for clinical trials in Australia and New Zealand.
A CTMS made with you, for you.
Working with you, Clinibase will fully customise our CTMS solution to fulfil your organisation's needs, providing ongoing troubleshooting and optimisation - ensuring a future proofed right fit.
More than 30 years of experience has taught us that there is no ‘one size fits all’ approach to clinical trial management systems. Each organisation has their own needs, systems, and processes. So why should your CTMS be any different?
We get it, and work with you to understand your situation, your targets, and goals, and aim to take the pressure off of finding, screening, and delivering participants directly into your calendar.
Software that optimises your experience, and the experience of your participants.
We ensure your CTMS system is as effortless as possible to set up and administer your clinical trial. By keeping across participant booking management, communication and activity tracking, your CTMS makes sure you always get your billings right.
Additionally, we drive increased participant retention rates through a strategy of personalised and automated communication, while fostering a positive participant experience all from your CTMS.
We put dynamic, usable data in your hands.
You can feel confident reporting results with improved tracking and real-time dashboards built on integrated electronic data capture (EDC), electronic source data (eSource) and electronic case report form (eCRF) workflows.
This visibility helps you monitor critical performance milestones, reduce missed visits and protocol deviations, optimise recruitment, and strengthen transparency between sites and sponsors.
What you can expect from Clinibase CTMS.
Clinibase CTMS supports sponsors and CROs with secure data management, streamlined participant administration, and clear performance insights. These capabilities give you reliable study oversight and help trials run accurately, efficiently and in line with protocol.
