VESO Vikan has extensive experience with trial design. Experimental challenge trials will be conducted according to prevailing regulations and guidelines and international standards.
VESO Vikan is certified according to GLP (Good Laboratory Practice) by Norwegian Accreditation and holds a manufacturing licence for medicinal products granted by the Norwegian Medicines Agency. VESO Vikan is certified to conduct potency- and safety studies of vaccines and pharmaceuticals for the European market according to GMP (Good Manufacturing Practice) requirements.
Trials in the laboratory and field can be performed according to GCP (Good Clinical Practice). Recently there has been an increased demand for aquatic medicine studies conducted according to high quality standards. GCP ensures international quality standards for clinical trials under the principles of the International Cooperation on Harmonization of Technical Requirements for Registration of Veterinary Medicinal Products (VICH). VESO Vikan also offers monitoring services for trials run according to GCP at other locations. For further information, please contact Audur Thorisdottir.