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