In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Aerosol OT 75 Drug Master File in Korea (Aerosol OT 75 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Aerosol OT 75. The MFDS reviews the Aerosol OT 75 KDMF as part of the drug registration process and uses the information provided in the Aerosol OT 75 KDMF to evaluate the safety and efficacy of the drug.
After submitting a Aerosol OT 75 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 Aerosol OT 75 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Aerosol OT 75 suppliers with KDMF on PharmaCompass.