In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Rogaine, Regaine, Avacor and Mintop, Minoxidil Drug Master File in Korea (Rogaine, Regaine, Avacor and Mintop, Minoxidil KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Rogaine, Regaine, Avacor and Mintop, Minoxidil. The MFDS reviews the Rogaine, Regaine, Avacor and Mintop, Minoxidil KDMF as part of the drug registration process and uses the information provided in the Rogaine, Regaine, Avacor and Mintop, Minoxidil KDMF to evaluate the safety and efficacy of the drug.
After submitting a Rogaine, Regaine, Avacor and Mintop, Minoxidil 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 Rogaine, Regaine, Avacor and Mintop, Minoxidil API can apply through the Korea Drug Master File (KDMF).
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