Financial & Business Association
of Euro-Asian Cooperation
On May 25, 2022 a round table was held within the framework of the Business Dialogues Program
On May 25, 2022 at 11.00 Moscow time, a round table was held within the framework of the Business Dialogues Program. The topic of the round table was "Features of registration of medical products in the territory of the Russian Federation and the EAEU".
The moderator of the event was CEO of LLC "First Integrated Registration Company" Dmitry Korobkin.
The round table was opened by the Acting President of the FBA EAC Alexander Kotlyarsky. He introduced the moderator and the initiator of the round table to the audience.
The event was attended by specialized companies from 6 countries of Eurasia.
Leading specialists of the First Integrated Registration Company LLC spoke about the requirements for registration of medical devices in the Russian Federation, about the features of registration of medical devices and products for in vitro diagnostics in the territory of the Russian Federation and the EAEU, shared their experience in auditing the quality management system of medical devices for compliance with the requirements of ISO 13485.
At the end of the round table Dmitry Korobkin answered the questions of the participants.
Summing up the results of the event, Alexander Kotlyarsky thanked the organizers, noting the relevance of the topic under consideration, the high professional level of the speakers and the interest of the audience specializing on the topic.
PRESENTATIONS
- FIRST COMPLEX REGISTRATION COMPANY
The moderator of the event was CEO of LLC "First Integrated Registration Company" Dmitry Korobkin.
The round table was opened by the Acting President of the FBA EAC Alexander Kotlyarsky. He introduced the moderator and the initiator of the round table to the audience.
The event was attended by specialized companies from 6 countries of Eurasia.
Leading specialists of the First Integrated Registration Company LLC spoke about the requirements for registration of medical devices in the Russian Federation, about the features of registration of medical devices and products for in vitro diagnostics in the territory of the Russian Federation and the EAEU, shared their experience in auditing the quality management system of medical devices for compliance with the requirements of ISO 13485.
At the end of the round table Dmitry Korobkin answered the questions of the participants.
Summing up the results of the event, Alexander Kotlyarsky thanked the organizers, noting the relevance of the topic under consideration, the high professional level of the speakers and the interest of the audience specializing on the topic.
PRESENTATIONS
- FIRST COMPLEX REGISTRATION COMPANY