Proposed amendments to the Regulations on Safety of Pharmaceuticals, etc.; (62 page(s), in Korean)

Application Process and Requirements for Post-Approval Changes of Biological Products Adopting the World Health Organization Guidelines for Changes to Approved Vaccines and Biotherapeutic Products for Human Use; (91 page(s), in English)

Draft amendments to the Rules for conducting clinical and clinical laboratory tests of medical devices; (75 page(s), in Russian)