In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a S4020,Sodium Picosulphate,10040-45-6 Drug Master File in Korea (S4020,Sodium Picosulphate,10040-45-6 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of S4020,Sodium Picosulphate,10040-45-6. The MFDS reviews the S4020,Sodium Picosulphate,10040-45-6 KDMF as part of the drug registration process and uses the information provided in the S4020,Sodium Picosulphate,10040-45-6 KDMF to evaluate the safety and efficacy of the drug.
After submitting a S4020,Sodium Picosulphate,10040-45-6 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 S4020,Sodium Picosulphate,10040-45-6 API can apply through the Korea Drug Master File (KDMF).
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