On January 15, Mr. Chen, a senior instructor from Deda, delivered an online lecture titled "Metrological Traceability and Uncertainty Calculation for In Vitro Diagnostic Reagents". During the online session, participants engaged actively, with the webinar fully attended. Mr. Chen elaborated thoroughly on the subject and patiently answered all attendees' questions, winning high appreciation from participants. More practical and informative training sessions are expected to be held in the future.
Brief Introduction to South Korea Medical Device Regulations
Analysis of South Korea Medical Device Registration Procedures
Technical Documentation Requirements for South Korea Registration
Differences in Medical Device Registration between China and South Korea
Date: Wednesday, April 1, 2026, 14:00 – 15:00
Format: Online Webinar
Benefit for Participants: Free live streaming
Organizer: CIRS Group – Beijing CIRS Technology Co., Ltd.
Contact: Manager Yan / Hangzhou Tel: 0571-87206527 / Beijing Tel: 010-63984062 / E-mail: MD@CIRS-GROUP.COM
Master of Dentistry, Yonsei University College of Dentistry; Expert in medical device regulatory affairs.
He possesses practical experience covering the full lifecycle of medical devices including testing, certification audit and regulatory consultation. He previously worked at MFDS-designated testing laboratories, the Certification Division of National Institute of Medical Device Safety Information (NIDS), and Osong Medical Innovation Foundation affiliated with the Ministry of Health and Welfare of Republic of Korea. He has accumulated abundant experience in medical device testing, registration & certification review, regulatory service and national-level project administration.
He holds review qualifications for technical documentation of various product categories: disposable supplies (surgical instruments, dental materials, cardiovascular implants, drug delivery devices) and electrical medical devices (physical therapy equipment, medical magnetic field generators, infusion devices). He can provide full-cycle professional consulting for medical devices intending to access the South Korean market.
Scan the QR code below via WeChat or click the link to sign up:
Registration Link：HTTPS://ZHN6M.XETLK.COM/SL/38GAIJ
Notes: Please complete all required information accurately with valid contact details. Reminders for webinar access will be sent prior to the event.
Changzhou Deda Kangcheng Medical Technology Co., Ltd.
Founded in 2014, Deda Medical specializes in pre-market regulatory and technical consulting services for medical devices. Its core businesses cover product registration, clinical trial, equivalent device evaluation, overseas registration, import registration, QMS establishment & maintenance, technology transfer, medical-industrial transformation and proof-of-concept verification.
Nearly a decade of steady development has enabled Deda to assemble an experienced and dynamic service team with solid industrial practical capabilities, alongside long-term cooperative partnerships with numerous domestic clinical institutions and testing laboratories. Committed to providing one-stop customized steward-style services, Deda helps clients mitigate registration risks, shorten project lead times and accelerate product market launch.
