Partner With Us
Your Research. Our Expertise.
Why Sponsors and CROs Choose Us
Rapid Study Start-Up
Average activation time under 60 days, from feasibility to first participant in, enabling faster trial launches and reduced operational delays.
High Enrolment & Retention
We maintain strong recruitment and retention rates through participant-centred processes and established referral networks. Explore our recruitment capabilities.
Phase I Oncology Expertise
Proven capability in early-phase oncology trials, including first-in-human, dose escalation, and pharmacokinetic studies.
Complex Trial Capability
Experienced in running complex trials involving genetically modified organisms (GMOs), cell and gene therapies, and novel combination regimens.
Experienced Clinical Team
Led by dedicated Principal Investigators and supported by study coordinators, research assistants, and research nurses.
Regulatory & HREC Support
Full support for regulatory submissions, ethics applications, and start-up documentation, ensuring efficient study approval processes.
Feasibility & Site Qualification
Quick turnaround on feasibility responses and robust site qualification materials to support your selection process.
Pharmacy & IMP Management
On-site pharmacy services for investigational product handling, including hazardous agents and temperature-sensitive biologics.
Imaging & Lab Partnerships
Integrated partnerships with accredited imaging centres and laboratories, supporting advanced diagnostics, and sample logistics.
Our Facilities
Purpose-Built for Oncology Research.
Our clinical trial unit is designed to support the delivery of high-quality, compliant oncology studies. We provide a professional, well-equipped environment for both patients and study partners, with facilities that meet the operational and regulatory needs of clinical research.
Contact us today to discuss your trial.
Send us an email to [email protected].
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Questions About Partnering With Us?
Explore our Sponsor FAQ for key information on trial setup and collaboration.