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