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