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Event Details


Medical Device Regulation in the Eurasion Union, Russia and the CIS

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Who should attend?

This seminar will be of particular interest to: Personnel working in medical device regulatory affairs in this region Anyone who is considering marketing a medical device in this region Those interested in an update of recent developments



The aim of this seminar is to provide a comprehensive overview of medical device regulatory affairs in Russia and the Eurasian Union. This interactive meeting will discuss the regulatory requirements within these regions. The focus will be on practical aspects to assist in developing your regulatory strategy for product approval in these countries. The presentations will also give practical hints on the regulatory and registration process where possible.


Attending this programme will:

  • Give you the full background to the CIS medical device market
  • Ensure that you understand the full implications of the new regulations which will affect how you do business in the Eurasian Economic Union (EAEU)
  • Help clarify the document requirements and timelines of national procedures and EAEU registration procedures
  • Fully update you on the national regulations in Russia, Belarus, Kazakhstan, Ukraine and other CIS countries


GBP EUR USD Standard 1499 2099 2338 Excluding VAT @ 20.00%


Leigh White

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