VESO has extensive experience with trial design. Challenge trials will be conducted in accordance with prevailing regulations and guidelines and international standards.
VESO Vikan is certified according to GLP (Good Laboratory Practice) by Norwegian Accreditation. We also hold a licence for medicinal products granted by the Norwegian Medicines Agency (NoMA) to conduct potency- and safety studies of vaccines and pharmaceuticals according to GMP (Good Manufacturing Practice) requirements.
Trials in the laboratory and field can be performed according to GCP (Good Clinical Practice). GCP ensures international quality standards for clinical trials under the principles of VICH (the International Cooperation on Harmonization of Technical Requirements for Registration of Veterinary Medicinal Products). VESO Vikan also offers monitoring services for trials run according to GCP by external partners.
Trials in Chile are conducted according to the same high-quality standards as in Norway.
For further information, please contact Audur Thorisdottir.