In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
										Pharmaceutical companies submit a 1,3,7-trimethyl-1H-purine-2,6(3H,7H)-dione Drug Master File in Korea (1,3,7-trimethyl-1H-purine-2,6(3H,7H)-dione KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 1,3,7-trimethyl-1H-purine-2,6(3H,7H)-dione. The MFDS reviews the 1,3,7-trimethyl-1H-purine-2,6(3H,7H)-dione KDMF as part of the drug registration process and uses the information provided in the 1,3,7-trimethyl-1H-purine-2,6(3H,7H)-dione KDMF to evaluate the safety and efficacy of the drug.
										After submitting a 1,3,7-trimethyl-1H-purine-2,6(3H,7H)-dione 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 1,3,7-trimethyl-1H-purine-2,6(3H,7H)-dione API can apply through the Korea Drug Master File (KDMF).
										click here to find a list of 1,3,7-trimethyl-1H-purine-2,6(3H,7H)-dione suppliers with KDMF on PharmaCompass.