Charles River can conduct single-site clinical trials at our facilities in both Scotland and Ireland. In particular, our research farm in Scotland has over 50 hectares of grazing and in excess of 5,000m2 of animal accommodation.
In addition, a wide range of pharmaceutical study types have been performed at our research facilities. Our parasitological experience includes efficacy, tolerance, dose determination, dose confirmation and developmental studies (e.g., dose delivery systems) using both endo- and ectoparasites.
We also have extensive experience managing multi-site field efficacy and field safety clinical trials throughout Europe in livestock and poultry.
Charles River offers a complete animal health product development service, including:
- Regulatory trial approval (e.g., ATC)
- Protocol and case report form (CRF) design
- Investigator selection and training
- External laboratory facilities selection and monitoring
- Project management
- Study monitoring
- Adverse event responses
- Drug supply and management
- Quality assurance
- Production of the final study report
Veterinary clinical studies are run according to VICH/GCP (v) guidelines and are supported by in-house quality assurance and statistics teams.
For more information about our clinical trials to support animal health product development, contact us at 1.877.CRIVER.1 or askcharlesriver@crl.com.