Proposed amendments to the Regulations on GMP for Medicinal Products; (161 page(s), in Korean)

Guidelines on the Recall of Health Products Regulated by the Food and Drug Administration; (13 page(s), in English)

Draft Amendments to Article 7 and to the Annex to Article 4 of the "Regulations Governing the Classification of Medical Devices"; (43 page(s), in English), (27 page(s), in Chinese)