Exposure to active pharmaceutical ingredients via any prescribed use of a veterinary medicinal product (VMP), carries potential risk and can be harmful to the environment.
Therefore, the authorisation process for VMPs requires an environmental risk assessment to evaluate the potential impact.
However, this process can be highly involved and may take significant time, creating delays before authorisation is achieved.
Our multi disciplinary team possess in-depth expertise across a range of industries and will work with you from initial study design to review.
You will have direct communication with your study director throughout the duration of your project, ensuring that you are consistently informed about its progress.
We offer a wide range of studies to the animal health industry, including:
Marine and freshwater species testing
Acute & Chronic packages
Higher Tier simulation studies