Abstract
The most important condition for rational pharmacotherapy is the presence of an advising regulatory framework in the field of circulation of medicinal products of proper quality, since the necessary effect from medicinal products occurs only if the requirements for the entire supply chain are met. This article is devoted to the analysis of the current regulatory framework in the field of regulation of antitubercular drugs in the Kyrgyz Republic, in order to provide patients with high-quality and highly effective medicinal products, which consumers, manufacturers and distributors are interested.
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