In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a 023C2WHX2V Drug Master File in Korea (023C2WHX2V KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 023C2WHX2V. The MFDS reviews the 023C2WHX2V KDMF as part of the drug registration process and uses the information provided in the 023C2WHX2V KDMF to evaluate the safety and efficacy of the drug.
After submitting a 023C2WHX2V 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 023C2WHX2V API can apply through the Korea Drug Master File (KDMF).
click here to find a list of 023C2WHX2V suppliers with KDMF on PharmaCompass.