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