Choose NZCR
Experience and Performance
- 35+ years of combined research excellence in complex early phase clinical research across a wide range of therapeutic areas.
- 800+ early phase clinical trials, including 140+ First-in-Human trials
- Skilled, experienced team of research professionals, including key opinion leaders.
- Recognised leadership team with an international reputation for safety and quality.
- Global standing as a leading site to conduct umbrella/ adaptive design trials spanning healthy volunteers and patients under one protocol, across a wide range of indications.
Purpose Designed Facilities and Services
- Purpose built research units with 81 beds over two geographically distanced locations.
- On-site laboratory and pharmacy services.
- Large healthy participant and patient population database of over 120,000 potential participants.
- In-house recruitment across a vast range of populations and therapeutic areas.
- State-of-the-art participant lounge with amenities to allow remote working.
- Four locations throughout NZ with access to a population of 5 million+.
- Dedicated late-phase vaccine trial locations with Optimal Clinical Trials.
Operational Excellence and Regulatory Compliance
- Operating in a supportive regulatory environment with fast start-up timelines of 6 weeks. Without the requirement for a CTA or IND.
- Commitment to Quality – GCP compliant, FDA, CRO and externally audited.
The NZCR Advantage
WE HAVE THE EXPERIENCE AND EXPERTISE TO CONDUCT YOUR NEXT RESEARCH PROJECT
-
- World-renowned Principal Investigators.
-
- 800+ trials completed.
-
- 17,000 clinical trial participants dosed.
-
- 4-6-week startup timelines.
-
- Unmatched recruitment across therapeutic indications.
-
- Commitment to safety and quality.
CLINICAL TRIAL PROJECT SOLUTIONS
-
- Expertise in protocol design and consultation
-
- Dedicated Business Development team providing a central point of contact and efficient feasibility process. [link to contact details]
-
- Experience in guiding sponsors through NZ’s supportive regulatory environment.
-
- Dedicated Start-Up team providing expert guidance and support through the clinical trial start-up process.
-
- Flexibility in scheduling and attractive timelines from consultation to dosing.
Our Clients and Partners
