In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a SUPREP BOWEL PREP KIT-1 Drug Master File in Korea (SUPREP BOWEL PREP KIT-1 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of SUPREP BOWEL PREP KIT-1. The MFDS reviews the SUPREP BOWEL PREP KIT-1 KDMF as part of the drug registration process and uses the information provided in the SUPREP BOWEL PREP KIT-1 KDMF to evaluate the safety and efficacy of the drug.
After submitting a SUPREP BOWEL PREP KIT-1 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 SUPREP BOWEL PREP KIT-1 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of SUPREP BOWEL PREP KIT-1 suppliers with KDMF on PharmaCompass.