Open AccessFEATURES OF THE ORGANIZATION OF CLINICAL TRIALS OF NARCOTIC DRUGS IN RUSSIA
Author(s) -
G. N. Gildeeva,
Е. А. Ежова,
Д. В. Бутузова,
N. L. Mishchenko,
V. Y. Yurkov,
А. В. Тетенева,
Т. С. Агеева
Publication year - 2019
Publication title -
sibirskij medicinskij žurnal
Language(s) - English
Resource type - Journals
ISSN - 2073-8552
DOI - 10.29001/2073-8552-2019-34-2-152-158
Subject(s) - legislation , government (linguistics) , process (computing) , russian federation , narcotic drugs , narcotic , narcotic analgesics , business , risk analysis (engineering) , medicine , computer science , political science , law , psychiatry , pharmacology , economic policy , linguistics , emergency medicine , philosophy , morphine , operating system
The problem of ensuring the necessary level of availability of narcotic drugs (NLP) in the Russian Federation, especially in the framework of palliative medical care for oncological patients is the area of special and constant attention of the Government and civil society. Recently, a number of necessary changes of the legislation aimed at simplifying the procedures for prescribing and issuing NLP have been introduced, and the possibility of optimizing the rules for their storage and accounting as well as improving the methods for calculating the needs for such drugs are being actively discussed.As part of the import substitution program in Russia, the new dosage forms for NLP are under development. Such process is accompanied by clinical studies with a number of features that take into account the specific chemical composition of finished products.