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