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