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