Guidelines on the Publishing of Package Insert and Patient Information Leaflet of Registered Drug Products in the Food and Drug Administration (FDA) Verification Portal System; (3 page(s), in English)

Proposed amendments to the "Regulation on the Permission, Notification, Review, etc of Medical Devices"; (51 page(s), in Korean)

Administrative Provisions for the Record-filing of Internet Information Services for Drug and Medical Devices (Exposure Draft); (5 page(s), in Chinese)