We have long-time and valuable experience in experimental studies and regulatory fields for veterinary drugs on food-producing species. Non food-producing species can be also included in cooperation with other CROs.

 

We assist you in the development of tailored experimental studies for pre-clinical and clinical assessment of your veterinary drugs in compliance with GLP/GCP

 

We provide expertise on Part III and IV of your registration dossier, including risks assessment for the environmental exposure and user’s safety. Assistance on dossier preparation and VET e-submission can also be provided.