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