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