Abstract
The article provides an overview of methodical recommendations, rules and guidelines for conducting preclinical studies of general toxic effect of pharmacological substances on the basis of international requirements for research. The introduction of new drugs for veterinary use into civil circulation is preceded by set of scientific studies to assess their effectiveness and safety in accordance with modern requirements. At the same time, it is necessary to observe a certain order of research at various levels on the basis of international standards, the most important stage of which is the study of the toxic effect of pharmacological substance in preclinical conditions. Preclinical toxicological studies are carried out in order to exclude in animals of target species possible adverse effects of the drug in the course of clinical trials and their subsequent use in veterinary practice.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callMore From: Problems of Veterinary Sanitation, Hygiene and Ecology
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
