In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Heparin sodium 1,000 units in dextrose 5% in plastic container Drug Master File in Korea (Heparin sodium 1,000 units in dextrose 5% in plastic container KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Heparin sodium 1,000 units in dextrose 5% in plastic container. The MFDS reviews the Heparin sodium 1,000 units in dextrose 5% in plastic container KDMF as part of the drug registration process and uses the information provided in the Heparin sodium 1,000 units in dextrose 5% in plastic container KDMF to evaluate the safety and efficacy of the drug.
After submitting a Heparin sodium 1,000 units in dextrose 5% in plastic container 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 Heparin sodium 1,000 units in dextrose 5% in plastic container API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Heparin sodium 1,000 units in dextrose 5% in plastic container suppliers with KDMF on PharmaCompass.