The article is devoted to the consideration of issues related to the current state of the digitalization process in the field of state quality control of medicines in Russia. The functioning automated information systems and electronic re- sources that contribute to more effective and transparent conduct of control and supervisory measures in order to estab- lish the quality of medicines, as well as relevant regulatory legal acts, are analyzed. Special attention is paid to the diffi- culties of functioning of the system for monitoring the movement of medicines and the need to resolve existing prob- lems in this area.
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