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