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