In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Chloride, Potassium Drug Master File in Korea (Chloride, Potassium KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Chloride, Potassium. The MFDS reviews the Chloride, Potassium KDMF as part of the drug registration process and uses the information provided in the Chloride, Potassium KDMF to evaluate the safety and efficacy of the drug.
After submitting a Chloride, Potassium 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 Chloride, Potassium API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Chloride, Potassium suppliers with KDMF on PharmaCompass.