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