Abstract
The presented article describes the concept, principles, rules and stages of circulation of medicines in the Republic of Kazakhstan. We are talking about the procedure for conducting a coordinated policy in the field of circulation of medicines, taking into account mutual interest in ensuring guarantees of the safety, effectiveness and quality of medicines for the life and health of people, protecting the life and health of consumers of medicines, preventing actions misleading consumers. The impact of the current legislation of the Republic of Kazakhstan in the field of health care and pharmaceutical activities on legal relations arising during the passage of all stages of circulation of medicines was considered. The main problems in this area have been disclosed. The positive experience of some foreign countries with developed legislation in the field of health care and pharmaceutical activities is being studied.