Watch now: 2023 South Korea regulatory overview
Gain a greater understanding of the decision points involved with determining a marketing submission category, and examine the examples provided by the Ministry of Food and Drug Safety (MFDS).
Webinar date
Aug. 8, 2023
Speaker
DaYeon Choi, Quality & Regulatory Affairs Consultant
In this webinar, the presenter helps attendees develop a greater understanding of the decision points they might face when determining a marketing submission category.
Learning objectives
- Examine examples provided by the Ministry of Food and Drug Safety (MFDS)
- Discuss the evaluation information the MFDS suggests providing for each category
- Share practical information intended to equip manufacturers for future medical device marketing submissions
About the presenter
DaYeon Choi, Quality & Regulatory Affairs Consultant
DaYeon Choi has more than 6 years of experience in the medical device industry and is working as a Quality & Regulatory Affairs Consultant based on her experience in developing Korea MFDS, EU IVDD/IVDR strategies for market access and regulatory compliance and in vitro diagnostic medical device manufacturers targeting the global market.
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