Implementing Guidelines on the Registration of Chemical Pharmaceutical Products for Human Use Applied for Marketing Authorization in accordance with Administrative Order No. 2024- 0013 "General Rules and Regulations on the Registration of Pharmaceutical Products and Active Pharmaceutical Ingredients Intended for Human Use"; (100 page(s), in English)

Draft amendments to the Requirements for the implementation, maintenance and evaluation of the quality management system of medical devices, depending on the potential risk of their use (2 pages, in Russian); (2 page(s), in Russian)

Proposed amendments to the "Regulation on medical device group and class by group"; (32 page(s), in Korean)