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