Why Choose NZCR for Clinical Trial?

Physician led state-of- the -art research units with 70 beds over two locations.
Skilled, experienced team of research professionals
Operating in a supportive regulatory environment with fast start up timelines of 4- 6 weeks. There is also no requirement for IND and CTA in New Zealand.
Commitment to Quality – fully GCP Compliant, FDA and externally audited
35+ years of combined research excellence (as ACS and CCST) in complex early phase clinical research across a wide range of therapeutic areas.
Reliable recruitment across a wide range of populations and therapeutic areas
Recruitment as one entity across the two largest centers in NZ with access to a population of 5 million+
Large healthy participant and patient population databases with dedicated and successful recruitment teams
Global standing as a leading site to conduct umbrella/adaptive design studies spanning healthy volunteers and patients under one protocol across a wide range of indications
Onsite laboratory and pharmacy services

Experience in guiding clients through NZ’s supportive regulatory environment and ensuring fast clinical trial start up timelines.
Experience in protocol design and consultation
Dedicated Business Development team providing a central point of contact and efficient feasibility process. Our Trial start up associate is available to support our clients through the NZ clinical trial start up process.
With two research units located in Auckland and Christchurch, we can offer flexibility in scheduling and attractive timelines
NZCR works closely with all CROs operating in New Zealand, including:
IQVIA, Covance, Syneos, PRA/ICON, PPD, Novotech, Pharmaceutical Solutions and Southern Star.

Why NZCR?