11月 15, 2023 MRG Egypt , Meeting with our valued visitors from Guangdong Baihe Medical Technology Co., LTD 阅读更多 5月 5, 2021 SFDA’s Announcement For Extending Of Work Procedures For Medical Device Marketing Authorization (MDMA) requests 阅读更多 4月 30, 2021 SFDA’s Guidance On Review And Approval Of Artificial Intelligence (AI) And Big Data Based Medical Devices 阅读更多 1月 19, 2021 SFDA’s Requirements For Safe Use Of Mammography 阅读更多 1月 19, 2021 SFDA’s Requirements For Safe Use Of Medical Ultraviolet Radiation 阅读更多 1月 19, 2021 SFDA’s Guidance For Medical Device Maintenance Facilities 阅读更多 1月 14, 2021 SFDA’s Announcement About Detailed Fees For Updating Medical Device Marketing Authorization (MDMA) Applications. 阅读更多 1月 7, 2021 SFDA’s Draft Guidance of Requirements of Licensing Service Providers for Quality Assurance and Ionizing Radiation Measurements in Healthcare Facilities. 阅读更多 1月 7, 2021 SFDA’s Draft On Essential Requirements for Medical Radiation Protection Programs. 阅读更多 1月 7, 2021 SFDA’s Draft Guidance of Importation and Re-Exploration for Radioactive Materials Used In Medical Applications 阅读更多 1月 4, 2021 SFDA’s Project Draft Guidance of Import / Re-export Requirments for Medical Imaging Materials. 阅读更多 12月 29, 2020 SFDA’s Guidance on Importation Requirements of Medical Devices Intended for Demonstration or Training Purpose only. 阅读更多 12月 29, 2020 Extending deadline for receiving requests for Marketing Authorization Applications via GHTF route. 阅读更多 11月 25, 2020 SFDA’s Guidance on Import and Clearance Requirements for Particle Accelerators 阅读更多 11月 22, 2020 SFDA’s Guidance on Requirements of Shipments Clearance at Ports of Entry 阅读更多 11月 22, 2020 SFDA’s Guidance on Requirements for Medical Masks and Particulate Respirators 阅读更多 11月 22, 2020 SFDA’s Products Classification Guidance 阅读更多 11月 19, 2020 SFDA’s Quality Management System Auditing Organizations 阅读更多 通讯订阅 向我们发送时事通讯以获取更新 名字 邮件 继续，即表示您接受隐私政策
