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