Government Policy on the Regulation of Clinical Trials and Drug Registration in Russian Federation

Student: Saitova Anna

Educational Programme: Health Care Administration and Economics (Master)

Year of Graduation: 2020

The pharmaceutical industry is a vital sector of the entire world economy and one of the key sectors of the economy of almost every country. Given the obvious importance of the industry, there is little research into the problems of state regulation of the pharmaceutical market, aimed at improving the quality of manufactured drugs. Therefore, in this paper, we consider the main problems of state regulation of clinical trials and drug registration in the Russian Federation, and also suggests ways to solve them.

Student Theses at HSE must be completed in accordance with the University Rules and regulations specified by each educational programme.

Summaries of all theses must be published and made freely available on the HSE website.

The full text of a thesis can be published in open access on the HSE website only if the authoring student (copyright holder) agrees, or, if the thesis was written by a team of students, if all the co-authors (copyright holders) agree. After a thesis is published on the HSE website, it obtains the status of an online publication.

Student theses are objects of copyright and their use is subject to limitations in accordance with the Russian Federation’s law on intellectual property.

In the event that a thesis is quoted or otherwise used, reference to the author’s name and the source of quotation is required.

Search all student theses