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Organization of Regulatory and Clinical Associates
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Organization of Regulatory and Clinical Associates
P.O. Box 3490
Redmond, WA 98073
(206)464-0825
HomeCurrent/Future EventsRecording - Medical Device and IVD Product Registration in Russia/Single Market Within Eurasian Econ

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Recording - Medical Device and IVD Product Registration in Russia/Single Market Within Eurasian Econ

When:
Tuesday, April 25, 2023
Where:
WA  

Contact:
ORCA Admin
Category:
Recording
Registration is required
Payment In Advance Only
This recording will be available for viewing until April 25, 2023.
Registrants & Fees
No Fee
No Fee
No Fee
$40.00

This is a recording of the April 25, 2018 webinar meeting.
Once current membership status has been confirmed, an email will be sent with a link to the recording.
If you are not a current member, the link will be sent to you via email after payment has been processed.
This recording will be available for viewing until April 25, 2023.


TOPICS: Medical Device and IVD Product Registration in Russia/Single Market Within Eurasian Economic Union (Russia, Kazakhstan, Belarus, Kyrgyzstan, Armenia)

TOPICS SUMMARIES: 
Medical Device and IVD Product Registration in Russia - Current Procedure
-Market overview (size, facts, figures)
-Basic registration analysis
-Legislation framework
-Classification rules
-Registration process depending on risk class
-Required documents
-Basic understanding of pre-clinical and clinical trials
-Duplicates of and amendments to the existing registration certificate
-Declaration issues

Single Market of Medical Device and IVD Product Within Eurasian Economic Union (RUS, BEL, KAZ, ARM, KYG) - Expected Changes
-Transition period clarification
-Legislation base
-Essential requirements of safety and performance
-Applied classification
-Basic understanding of registration process
-Quality Management System requirements
-Safety monitoring (surveillance)
-Comparison of current registration in Russia and EEU procedures
-Critical points of single market


SPEAKERS: Tatiana Nosova, Ruslan Kalachev (BeAWire)

SPEAKERS BIOS: 
Tatiana Nosova is the CEO at BeAWire Regulatory Affairs Agency. Mrs. Nosova has a M.Sc. in Biomedical Engineering from the Bauman Moscow State Technical University. After graduation, she worked as an RA specialist and then as a Head of RA Department in medical device companies. In the last company she established this activity as new area of company scope. Vast number of manufacturers successfully registered their products under her guidance: Penumbra Inc., Intuitive Surgical Inc. (da Vinci Surgical System), Terumo Corporation, etc. Mrs. Nosova is involved in technical reviews and management of the company.

Ruslan Kalachev is the Director of Strategic Development at BeAWire Regulatory Affairs Agency, which specializes on medical device and IVD product registration in Russia. Mr. Kalachev has a Master Degree in Biomedical Engineering from the Bauman Moscow State Technical University. He worked as an engineer and a sales representative in medical devices companies. His mission in the company is to provide guidance to manufacturers worldwide with regards to the expected regulatory changes. Mr. Kalachev has been an invited speaker at many conferences worldwide (China, Germany, Japan, Korea, Netherlands, USA).