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