This veterinary drug good laboratory practice (GLP) aims to further strengthen the safety evaluation of veterinary drugs and ensure the safety and efficacy of veterinary drugs. The GLP specification consists of 48 Articles.
This GLP specification applies to non-clinical studies conducted for the registration of veterinary drugs. The non-clinical safety evaluation research institution of veterinary drugs shall follow this specification. The GLP specification provides for the requirements to be satisfied for organization and personnel; experimental facilities; equipment and experimental materials; standard operating procedures; implementation of research work; etc.