In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a 2-Propanol, technical grade, 95% Drug Master File in Korea (2-Propanol, technical grade, 95% KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 2-Propanol, technical grade, 95%. The MFDS reviews the 2-Propanol, technical grade, 95% KDMF as part of the drug registration process and uses the information provided in the 2-Propanol, technical grade, 95% KDMF to evaluate the safety and efficacy of the drug.
After submitting a 2-Propanol, technical grade, 95% 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 2-Propanol, technical grade, 95% API can apply through the Korea Drug Master File (KDMF).
click here to find a list of 2-Propanol, technical grade, 95% suppliers with KDMF on PharmaCompass.