January 14, 2021 SFDA’s Announcement About Detailed Fees For Updating Medical Device Marketing Authorization (MDMA) Applications. Read more January 7, 2021 SFDA’s Draft Guidance of Requirements of Licensing Service Providers for Quality Assurance and Ionizing Radiation Measurements in Healthcare Facilities. Read more January 7, 2021 SFDA’s Draft On Essential Requirements for Medical Radiation Protection Programs. Read more January 7, 2021 SFDA’s Draft Guidance of Importation and Re-Exploration for Radioactive Materials Used In Medical Applications Read more January 4, 2021 SFDA’s Project Draft Guidance of Import / Re-export Requirments for Medical Imaging Materials. Read more December 29, 2020 SFDA’s Guidance on Importation Requirements of Medical Devices Intended for Demonstration or Training Purpose only. Read more December 29, 2020 Extending deadline for receiving requests for Marketing Authorization Applications via GHTF route. Read more November 25, 2020 SFDA’s Guidance on Import and Clearance Requirements for Particle Accelerators Read more November 22, 2020 SFDA’s Guidance on Requirements of Shipments Clearance at Ports of Entry Read more November 22, 2020 SFDA’s Guidance on Requirements for Medical Masks and Particulate Respirators Read more November 22, 2020 SFDA’s Products Classification Guidance Read more November 19, 2020 SFDA’s Quality Management System Auditing Organizations Read more
