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