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