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Benefits for international multicenter clinical trials in Russia

Thursday, September 1, 2016

In the last 20 years, Russia has seen an increasing growth of the clinical trials industry. Among the factors contributing to that are top-grade research facilities, vast and easy-to-access populations and low participation costs. Over the past two years, significant changes have occurred in this market that are likely to have a global impact. All recent legislative efforts were aimed at harmonizing the local regulatory requirements with international standards and pharmacovigilance procedures. Clinical trials in Russia undergo regular FDA inspections and are among one of the world’s best in terms of quality, exceeding Western countries.

In the light of these changes, Russia is now seen also as a gate­way to the market of the Eurasion Economic Union (EEU) for inter­national companies. The EEU and EU legislations are very similar. The EEU pharmaceutical registration procedure requires the submission of the following clinical trial reports:

  • Clinical trials conducted in ICH regions or within the EEU before January 1, 2016.
  • Clinical trials conducted in one or all EEU member states in compliance with applicable EEU regulations after January 1, 2016.

These requirements make a com­pany’s GCP/GLP compliance, audit results and general experience partic­ularly important criteria in the selec­tion of CROs. Nevertheless, there are many issues that still require clarifica­tion. This, however, gives pharmaceu­tical companies the needed breathing space to make all the necessary prep­arations for the new procedure.

Global market research shows that in 2015, the share of internation­al multicenter clinical trials did not change as compared to the previous period, and amounts to about 38%. Having become the stepping stone for entering into new markets, Rus­sia is expected to raise even more interest from international phar­maceutical companies as the most important region for international multicenter clinical trials.

 

Written by Guest Writer Dmitry Sharov. Sharov, OCT president, has over 15 years’ experience in clinical trials. More than 10 years ago, Dmitry founded OCT, a clinical research organization that now employs more than 150 professionals and has the largest team of medical writers and most experienced regulatory experts. As a dedicated leader, Dmitry is responsible for establishing the corporate vision and business development strategies.

This article was reprinted from Volume 23, Issue 09, of The CenterWatch Monthly, an industry leading publication providing hard-hitting, authoritative business and financial coverage of the clinical research space. The Action Items section features short columns  focusing on actionable or how-to advice from clinical trial professionals. To submit an Action Item, please contact editorial@centerwatch.com. Subscribe >>

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