Know the Global, International and Public Health Policy, Health Systems Management, Management Economics, Pharmaceutical Economics and Pharmaceutical Policy, Pharmaceutical Oversight, Pharmaceutical Quality Management, Drug Authorization, Clinical Research Business Administration, Pharmaceutical Supervision and Pharmaceuticals;

Know the management, incl. features of the management process of the organization, the universal functions of pharmaceutical management, teamwork and leadership, decision making, decision making and implementation stages, which lead to the development of new ideas or proposals for the management of the system, each segment of the field of pharmaceutical management and statistical processing characteristics;

Have s systematic knowledge of pharmaceutical quality management system, in particular, will understand GMP API (Good Manufacturing Practice of Active Pharmaceutical Product), GMP MP (Good Manufacturing Practice of Medicinal Product), GDP API (Good Distribution Practice of Active Pharmaceutical Product), GDP MP (Good Distribution Practice of Medicinal Product) GDP Exipien (Good Distribution Practice of Excipient), GSP (Good Storage Practice), quality Correction And Process Assurance (CAPA) system, through which it will understand ways to solve drug safety, quality, efficacy problems at the production, distribution and logistics stages;

Know the correct clinical practice (GCP) and ethical principles of research (well-being of research subjects, etc.);

Understand specific pricing strategies  (including cartel transactions, price leadership, discrimination, unlimited pricing).

Formulate and control the organization of healthcare, mission and goals of pharmaceuticals, strategic and current plans (including quality management), marketing of pharmaceutical products, organization of work and human resources, management and control of work under the plan;

Plan, implement and audit the systemic activities of multidisciplinary quality assurance and correction (CAPA) at the stage of distribution of the pharmaceutical product, as well as have an ability of strategic planning of the projected side effects of the drugs consumed, clinical research administration, business plan design, strategic planning;

Solve complex problems arising during the administration process (well-being of the clinical research subject, compensation, violation of standard information procedures, etc.) with new approaches, processing of research results with the latest statistical methods and approaches;

Formulate a reasoned opinion on the systematic level of innovative information synthesis and critical analysis of data on the results of complex information and computational covariance and correlation in pharmaceutical systems, pharmaceutical structures, pharmaceutical markets and research;

Process statistically the data on the innovative synthesis of complex information and computed covariance and correlation results in pharmaceutical structures, pharmaceutical market and research, form a reasoned opinion about their critical analysis at the systemic level of health;

Evaluate the system based on a critical analysis of processes provided by the GMP MP (Good Manufacturing Practice of Medicinal Product) and GMP API /(Good Manufacturing Practice of Active Pharmaceutical Product);

Formulate a final assessment based on a critical analysis of complex modular information (safety, quality, efficacy, legality, ethical aspects of the pharmaceutical industry);

Make reasoned decisions based on the validity of regulatory models / instruments and the rationality of pharmacotherapy based on a critical analysis of the latest data on pharmaceutical policy and pharmacoeconomics.

Strategically plan and study Healthcare, incl. pharmaceutical management, supervision, drug authorization, research, quality system as a dynamically developing field, the need for further in-depth study, and independent study of individual issues (including statistical-mathematical);

Assess the social corporate responsibility of the pharmaceutical entity to the public, as well as promote the principles of managerial, medical, pharmaceutical ethics in the provision of health services;

Assess the advantages of standardized management over the principles of directive management and to promote its establishment, as well as to assess the attitudes of self and health professionals in the ethics of drug use, research and pharmacy in general.;