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.

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.

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.

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

Whether you're looking for a marketing study, or studies completed to Good Clinical Practice (GCP) or Good Laboratory Practice (GLP), we can do them all — from residue studies and target animal safety to field efficacy studies, dose confirmation and tolerance, and pharmacokinetics (PK). Our experienced trial coordinators and technicians have meticulous attention to detail

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.

Our epidemiologists specialise in study design and process, delivering clear, defensible results. Whether it's efficacy, safety, residues, marketing or something else, our trial design draws on sample size calculations, bias control and recruitment strategies to ensure your study is built on strong scientific foundations.

There's no shortcut to a compliant product, but there is a smarter path through it. From regulatory plan and data support to ACVM registration support, we guide you from start to finish of your product development journey. With more than 25 years' combined experience registering new products, we advise on Chemistry and Manufacturing, Efficacy, Safety