In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Zinca 20 Drug Master File in Korea (Zinca 20 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Zinca 20. The MFDS reviews the Zinca 20 KDMF as part of the drug registration process and uses the information provided in the Zinca 20 KDMF to evaluate the safety and efficacy of the drug.
After submitting a Zinca 20 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 Zinca 20 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Zinca 20 suppliers with KDMF on PharmaCompass.