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