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