Two Day Seminar: Medical Device Regulation in the Eurasian Union, Russia and the CIS (London, United Kingdom - October 9-10, 2018) - ResearchAndMarkets.com
DUBLIN--(BUSINESS WIRE)--Jul 19, 2018--The “Medical Device Regulation in the Eurasian Union, Russia and the CIS” conference has been added to ResearchAndMarkets.com’s offering.
A comprehensive overview of medical device regulatory affairs in Russia and the Eurasian Union. Key countries covered include Armenia, Azerbaijan, Belarus, Georgia, Kazakhstan, Kyrgyzstan, Moldova, Russia, Tajikistan, Turkmenistan and Ukraine.
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
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
Day one - Russia
Russia - the competitive landscapeCurrent market and projected growth Health-2020 state program Localisation of manufacturing Pricing and reimbursement Patent and data protection
National standardsTechnical requirements and standards in key regions
Registration of medical devices in RussiaRegulatory authorities in Russia and key bodies Key regulations governing registration process Clinical trials for medical devices Registration procedures - what is required? Application dossier and data requirements Post approval life cycle maintenance applications Safety reporting and market surveillance
Day two - CIS and EAEU
CIS - Regional regulatory overviewCIS pharmaceutical market CIS in International Regulatory Harmonisation CIS regional regulatory co-operation - Eurasian Economic Union
Eurasian regulations for medical devicesCountries - members of EAEU, official bodies and terms of transition period EAEU data requirements EAEU registration procedures
Registration of medical devices in CISCommon regional requirements in CIS: Administrative data, translations, FSC, Dossier format, local Normative Document, samples, labelling Country specific requirements: Ukraine, Kazakhstan, Belarus, Moldova, Georgia, Armenia, Azerbaijan, Uzbekistan, Tajikistan, Turkmenistan, Kyrgyzstan
Practical workshopCIS Regional Regulatory Strategy
For more information about this conference visit https://www.researchandmarkets.com/research/ff6c4w/two_day_seminar?w=4
View source version on businesswire.com:https://www.businesswire.com/news/home/20180719005558/en/
Laura Wood, Senior Manager
For E.S.T Office Hours Call 1-917-300-0470
For U.S./CAN Toll Free Call 1-800-526-8630
For GMT Office Hours Call +353-1-416-8900
KEYWORD: UNITED KINGDOM EUROPE RUSSIA
INDUSTRY KEYWORD: HEALTH MEDICAL DEVICES
SOURCE: Research and Markets
Copyright Business Wire 2018.
PUB: 07/19/2018 10:52 AM/DISC: 07/19/2018 10:52 AM