Bringing an animal health product to market requires a detailed understanding of the regulatory landscape. At EpiVets, we support companies of all sizes through the entire product registration and compliance process so your innovation can progress without unnecessary delays.
Our team stays informed on the latest regulatory requirements across New Zealand and Australia. This includes APVMA, ACVM and other relevant frameworks that govern veterinary medicines, agricultural products, and animal health technologies. We help you understand what the regulations mean for your product and how best to meet them.
From early stage planning through to post approval compliance, we provide a practical and evidence based approach. Our regulatory specialists work closely with our research and trial teams to ensure the information generated for your dossier is robust, accurate, and aligned with current expectations. As a GLP accredited organisation, we understand the quality systems required to produce defensible data.
Whether you need support with data gap analysis, study planning, technical summaries, risk assessments, or full registration packages, EpiVets offers guidance at every step. Our goal is to help you avoid costly setbacks and maintain ongoing compliance throughout the life of your product. We have a proven track record of helping clients meet the needs of both regulators and end users, ensuring your product remains safe, effective, and trusted in the market.