Draft amendments to the Rules of classification of medical devices depending on the potential risk of use; (39 page(s), in Russian)

Draft Food and Drug Administration (FDA) Circular "Guidelines for the Importation and Exportation of Finished Drug Products and Raw Materials"; (6 page(s), in English)

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