Trial delivery, speed and quality

Speed & Quality

At ACTT, we understand the importance of speed during the feasibility and set up and we strive to ensure trial activation occurs as fast as possible.

• KPI 90 days to SIV ready
• Median contracting cycle time: 44 days
• Rapid FPI track record across multiple specialties
• Centralised contracting and budgeting

Centralised Start-up Team
With strong expertise in New Zealand requirements, we ensure all studies meet Health and Disability Ethics Committee (HDEC) and Medsafe regulatory standards, supporting timely approvals and full compliance.

By centralising these processes, we reduce start-up timelines, minimise administrative burden on investigators, and enable studies to commence smoothly and efficiently.

Recruitment

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Participant retention consistently above 90%
Nationwide access to inpatient and outpatient populations

How we work with our investigators

We work in partnership with highly experienced Subject matter experts (SMEs) across a broad range of therapeutic areas, bringing deep clinical expertise and strong research leadership to every study.

Our SMEs are respected specialists within their fields, actively contributing to clinical practice, research innovation, and the advancement of evidence-based medicine in Aotearoa New Zealand and internationally.

Each trial also has a Project Agreement in place – between the Principal Investigator and ACTT. 

This agreement confirms:

• Details of the trial including site staffing and sub-investigators
• The target number of participants
• The recruitment timelines
• A recruitment plan to ensure that the target is met