We can guide and support you from start to finish of your product development journey. With our expertise and more than 25 years’ combined experience in registering new products, we can advise on Chemistry and Manufacturing, Efficacy, Safety and Residues requirements, meet with regulators, help you build your registration data package and shepherd it through the assessment and approval process, ensuring your product will be compliant with local regulations.

Our epidemiologists design studies that deliver clear, defensible results. Whether it’s efficacy, safety, residues, marketing or something else, from sample size calculations to bias control and recruitment strategies, we ensure your trial is built on strong scientific foundations.

Every study involving animals requires an animal ethics approval. We manage the entire ethics process through Tika Ethics, our independent Animal Ethics Committee. This enables a more seamless approach to approvals while ensuring full compliance with New Zealand’s Animal Welfare Act and the Three Rs.

Access to suitable farm locations, animals, farmers and veterinarians is critical for conducting your research objectives. We utilise our extensive national and international network of commercial farms and vets to identify and coordinate the right locations for you to do your research.

Whether you are looking for a marketing study, or studies completed to Good Clinical Practice (GCP) or Good Laboratory Practice (GLP) – we can do them all. Our experienced trial coordinators and technicians have meticulous attention to detail in combination with practicality, ensuring credibility and compliance at every stage.

We turn complex trial data into clear, defensible insights. Our epidemiology-led approach ensures robust and efficient data collection, data management, and advanced analytics to support product registration and decision-making. 

Clear and comprehensive reporting is vital to demonstrate the value of your product. We compile detailed reports that meet regulatory and scientific standards, and if needed, provide extensions to refine or expand on findings. This ensures your product's development is well-documented and adaptable.

The final step in bringing your product to market is its official registration. Whether for ACVM or APVMA, we prepare and submit a comprehensive data package, liaising with regulatory authorities to ensure a smooth review and approval process. This step formalises your product’s entry into the market with confidence and compliance.