With nearly 40 years of experience serving leaders in medical device technology, our team is dedicated to lifting every aspect of your trial, from early protocol design to speedy approvals, data monitoring & collection and beyond. We combine an Australia-based CRO foundation with global reach, and CRC's available across Australia, New Zealand, & Asia, ensuring we meet the requirements for US FDA Clinical Trials, European CE mark and other international regulations.
Why work with us
A+ team delivers A+ service:
Evolving upwards together. Lifting up the research, the team, and most of all, patients’ lives.
Our objective is to offer an end-to-end solution tailored to the needs of medical device companies. We ensure that your clinical trial is supported by a distinguished and highly experienced project team capable of adapting to your evolving requirements and collaborating seamlessly with all chosen partners to synchronise cross-functional efforts, ultimately guiding your project along a strategic pathway to success.
