01 1SK Biotek Ireland Limited
01 1Korea BMS Pharmaceutical Co., Ltd.
01 1Atazanavir sulfate
01 1U.S.A
Registrant Name : Korea BMS Pharmaceutical Co., Ltd.
Registration Date : 2009-08-21
Registration Number : Su335-4-ND
Manufacturer Name : SK Biotek Ireland Limited
Manufacturer Address : Watery Lane, Swords, County Dublin
74
PharmaCompass offers a list of Atazanavir Sulfate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Atazanavir Sulfate manufacturer or Atazanavir Sulfate supplier for your needs.
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A ATAZANAVIR SULPHATE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ATAZANAVIR SULPHATE, including repackagers and relabelers. The FDA regulates ATAZANAVIR SULPHATE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ATAZANAVIR SULPHATE API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of ATAZANAVIR SULPHATE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A ATAZANAVIR SULPHATE supplier is an individual or a company that provides ATAZANAVIR SULPHATE active pharmaceutical ingredient (API) or ATAZANAVIR SULPHATE finished formulations upon request. The ATAZANAVIR SULPHATE suppliers may include ATAZANAVIR SULPHATE API manufacturers, exporters, distributors and traders.
click here to find a list of ATAZANAVIR SULPHATE suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a ATAZANAVIR SULPHATE Drug Master File in Korea (ATAZANAVIR SULPHATE KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of ATAZANAVIR SULPHATE. The MFDS reviews the ATAZANAVIR SULPHATE KDMF as part of the drug registration process and uses the information provided in the ATAZANAVIR SULPHATE KDMF to evaluate the safety and efficacy of the drug.
After submitting a ATAZANAVIR SULPHATE 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 ATAZANAVIR SULPHATE API can apply through the Korea Drug Master File (KDMF).
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