•        Demonstrates knowledge of pharmaceutical economics and pharmaceutical policy, pharmaceutical quality systems management, drug authorization, business administration of clinical trials, pharmacovigilance and pharmaceutical ethics, global, international and public health protection policy, health systems management, managerial economics;

·         Understands the universal functions of pharmacy management, teamwork, leadership, management, etc. features of the healthcare organization's management process, receiving quantitative and qualitative information and statistical processing;

•        Understands GMP API (Good Manufacturing Practice for Active Ingredient), GMP MP (Good Manufacturing Practice for Pharmaceutical Product), GDP API (Good Distribution Practice for Active Ingredient), GDP MP (Good Distribution Practice for Pharmaceutical Product), GDP Exipien (Good Distribution Practice for Excipients) ), GSP (good warehousing practice) and quality process prevention and correction (CAPA) system, through which it solves the problems of safety, quality, efficiency of drugs at the stage of production, distribution and logistics;

•        Describes and defines issues of good clinical practice (GCP), ethical principles of research (welfare of research subjects, etc.), specific pricing strategies (including cartel bargaining, price leadership, discrimination, unlimited pricing);

•        Formulates and determines the mission and goals of pharmaceutical activity entities, health care organization, strategic and current plans (including quality system management), marketing of pharmaceutical production, methods of organization, coordination and control of work to be carried out;

•        Plans and implements systematic activities of multidisciplinary prevention and correction (CAPA) of quality assurance at the stage of pharmaceutical product distribution, produces unintended side effects of consumed drugs, administration of clinical trials, drawing up a research business plan and financial calculations;

•        On the basis of critical analysis, formulates justified conclusions at the system level of health care, pharmaceutical structures, pharmaceutical market and research by innovative synthesis of complex information and statistical data processing of calculated covariation and correlation results;

•        Collects, processes, interprets and evaluates complex modular drug information (safety, quality, effectiveness, legality, ethical aspects of pharmaceutical industry actions);

•        Develops sound initiatives based on critical analysis of the latest pharmaceutical policy and pharmacoeconomics data, validity of regulatory models/tools and rationality of pharmacotherapy;

•        Evaluates the social corporate responsibility of the pharmaceutical entity to the society, the superiority of the administration under the supervision of standards in relation to the principles of directive management and promotes its establishment, the development of the principles of managerial, medical, pharmaceutical ethics in the provision of healthcare services, as well as evaluates the attitude of oneself and healthcare professionals in the ethics of drug use, research and pharmacy in general;

•        Understands health care, including pharmacy management, supervision, drug authorization, research, quality system as a dynamically developing field, the need for further in-depth study and independent planning of separate issues (including in the statistical-mathematical field);