Authors: E L Kovaleva V L Bagirova L I Mitʼkina O A Matveeva E R Akopova N A Vinogradova
Publish Date: 2010/04/13
Volume: 43, Issue: 12, Pages: 668-676
Abstract
The status of “observer” received by Russia in the European Pharmacopoeia Commission provides an opportunity to use materials of Ph Eur However there is no description of finished pharmaceutical dosage forms in Ph Eur Therefore it is necessary to develop national approaches to evaluation of the quality efficacy and safety of medicines that conform to the international level of requirements The article is dedicated to the problem of standardization of medicines in the pharmaceutical dosage form “tablets” that are intended for oral administration
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