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