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