GCA KOREA (380) 썸네일형 리스트형 MFDS Revises CGMP to Align with International Standards Korea MFDS UpdatesThe Ministry of Food and Drug Safety (MFDS) has updated the "Cosmetic Good Manufacturing Practice (CGMP)" to better align with international standards, including ISO 22716. This revision aims to simplify export processes for domestic cosmetics manufacturers by ensuring compliance with globally recognized GMP standards.You can find detailed information on the latest Korean MFDS .. KC Certification Classification of Conformity Assessment In South Korea, KC Certification is essential for ensuring that equipment related to the radio environment and communication networks meets safety and performance standards. Depending on the level of risk and the type of equipment, manufacturers, sellers, and importers must follow different conformity assessment. KC Conformity CertificationAnyone who intends to manufacture, sell, or import equip.. Korea's National Intellectual Property Commission publishes report on artificial intelligence and IPR The Presidential Council on Intellectual Property has released a comprehensive report on the current state of large-scale AI. It explores the impact of AI on intellectual property, the challenges it presents, and the need for new legal frameworks as AI technology evolves.Highlights:Research Directions: New agendas for AI-related intellectual property.Focus on Generative AI: Analysis of technolog.. South Korea Launches National AI Research Hub to Become a Global Leader South Korea is making bold moves to become one of the world's top three AI powerhouses. The Ministry of Science and ICT, along with IITP, has chosen a consortium of KAIST, Korea University, Yonsei University, and POSTECH to lead the creation of a national AI research hub in Seoul.This hub will be located in Seoul's AI center, covering 7,050.5 square meters. It will bring together universities, l.. MFDS July 2024 Medical Product Approval Update: 126 Items Approved Korea MFDS UpdatesIn July 2024, the Ministry of Food and Drug Safety (MFDS) approved a total of 126 medical product items. These approvals include: • 22 Pharmaceuticals • 2 Quasi-drugs • 102 Medical Devices Curious about how the July medical product approvals compare to last month or last year? Check out the details, along with more information on the latest regulations and updates regarding Kor.. The transfer of the Computer Energy Efficiency Management System is planned The transfer of the Computer Energy Efficiency Management System is planned Starting from January 1, 2025, the production (import) and sale of computers that do not meet the minimum energy efficiency standards will be prohibited. Additionally, an efficiency label (indicating compliance with minimum energy efficiency standards) must be affixed to the products. Scope of Application:This regulation.. KC EMC Certification Marking The following marking requirements apply to equipment that has received KC EMC certification: 1. Equipment with Certification of Conformity, Registration of Conformity, Interim of ConformitySuch equipment must have the conformity assessment marking (including the KC mark, certification or registration number, company name, product name, model number, manufacturing date, manufacturer, and country.. Opening of the 19th International Standards Olympiad Opening of the 19th International Standards Olympiad The world’s only international standards competition for youth, aimed at nurturing future talent, has begun. The Korean Agency for Technology and Standards announced the 19th International Standards Olympiad finals, with 120 students from 11 countries, including Korea, Japan, China, and Singapore. This year's International Standards Olympiad s.. Korean MFDS Amends the Medical Device Act Enforcement Rules On August 7, the Ministry of Food and Drug Safety (MFDS) made significant revisions to the Medical Device Act Enforcement Rules. These updates, effective from August 7, 2024, bring several key changes. 🔹 All Class 1 medical devices will be unified under a notification system. 🔹 Exemptions from clinical trial plan approvals will be expanded. 🔹 Participation criteria for non-clinical trial inst.. Post-Market Surveillance for Conformity Assessment Post-Market Surveillance for Conformity Assessment Products distributed in the market are collected and tested for compliance with technical conformity assessment standards. Through monitoring activities such as field investigations, compliance with obligations is examined, and administrative actions are taken in cases of violations. - Compliance with Technical Standards for Conformity Assessmen.. 이전 1 ··· 6 7 8 9 10 11 12 ··· 38 다음
