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