Abstract:
The aim of the study is to review the historical stages of development of the requirements of good pharmaceutical
practice (GPP), generalization of the normative documents recommended by the International pharmaceutical
company (MFP) for use in the world of pharmaceutical practice. Methods of generalization of the information
material and system analysis were used in the study. Historical stages of the development of the concept of
the GPP in the world and the role of the World Health Organization and the FIP in the process were analyzed.
Researches of professional standards of pharmacy practice in developed countries reveal different approaches
to the regulation of such activities, however, despite the applicable model standards are developed by the
pharmaceutical associations and are used by regulatory bodies, business owners, and professionals to control
the quality of pharmacy services that are provided to the population. The study indicates that the development of
the GPP standards should be resolved at the level of public professional organizations as the national regulation
of pharmacy practice in different countries varies significantly. Prospects of further scientific researches are
aimed on using the results of the study while developing and implementing national standards of the GPP in
the world.
