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