Abstract
Nowadays the doctor’s practice more and more involves not just the requirement to know clinical issues, but also the mandatory awareness of regulatory documentation. Formerly normative documents (federal laws, orders of different levels) were the prerogative of public health officials and heads of healthcare institutions. In recent years, the number of documents is increasing immensely, so that general practitioner is not able to keep track of all this data flow, although ignorance of normative documents causes various serious consequences. Moreover, regulatory documents at different levels (HМ of RF, local) are developed and ratified in large number meanwhile their quality leaves much to be desired though.
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