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