ARQon (Asia Regulatory & Quality Consultancy) and ARPA(Asia Regulatory Professionals Association) are launching the Medical Device School program to provide an ideal opportunity to MEDTECH INDUSTRY PROFESSIONALS to gain a comprehensive overview of medical devices lifecycle, from research and development stages to commercialization in Korea.
Date and time: 10am - 6pm (PST, Seoul), 8 Dec 2020
Venue: Online (Live)
Gain valuable insights and experiences from the key respected speakers in the field to apply to your work/decision and preventing common mistakes.
Gain a comprehensive understanding on global regulatory landscape and latest updates including the new CE MDR/IVDR enforcement by Dec 2020/2022.
Discover the design, testing and standards requirements for product safety.
To explore the advanced technologies in medical device.
To hear about the market strategies, opportunities and challenges in the manufacturing and distribution. Networking with Medtech partners and industries, for potential collaboration.