Medical Device Regulation in the Eurasian Union, Russia and the CIS
The aim of this event is to provide a comprehensive overview of medical device regulatory affairs in Russia and the Eurasian Union. This interactive course will cover the regulatory requirements within these regions, focusing on practical aspects to assist in developing your regulatory strategy for product approval. The presentations will also give practical hints on the regulatory and registration process where possible.
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Suitability - Who should attend?
Benefits of Attending
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
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Reviews by course attendees
Average rating 4.2
My opinion is overall very positive. I liked how the content was delivered and the knowledgeable speaker.
Great
Speaker was really good and easy to understand for a non-native english speaker as I am. Organization of webinar was perfect. The assistance attendent was here for us in case of...