In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a POTASSIUM CHLORIDE 0.22% IN DEXTROSE 5%; SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER-2 Drug Master File in Korea (POTASSIUM CHLORIDE 0.22% IN DEXTROSE 5%; SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER-2 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of POTASSIUM CHLORIDE 0.22% IN DEXTROSE 5%; SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER-2. The MFDS reviews the POTASSIUM CHLORIDE 0.22% IN DEXTROSE 5%; SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER-2 KDMF as part of the drug registration process and uses the information provided in the POTASSIUM CHLORIDE 0.22% IN DEXTROSE 5%; SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER-2 KDMF to evaluate the safety and efficacy of the drug.
After submitting a POTASSIUM CHLORIDE 0.22% IN DEXTROSE 5%; SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER-2 KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their POTASSIUM CHLORIDE 0.22% IN DEXTROSE 5%; SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER-2 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of POTASSIUM CHLORIDE 0.22% IN DEXTROSE 5%; SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER-2 suppliers with KDMF on PharmaCompass.