Law No. 12/2025 – Medical Device Supervision and Administration Regime; (42 page(s), in Portuguese), (42 page(s), in Chinese)

Proposed establishment of the "Regulations on the Approval of Clinical Trial protocols and Management of Conducting Clinical Trials for Digital Medical Devices"; (80 page(s), in Korean)

Proposed amendments to the "Specification and Test Methods for Biological Products"; (15 page(s), in Korean)