01 1Esteve Quimica, SA
02 1Yuhan Chemical Co., Ltd.
01 2Gilead Sciences Korea Ltd.
01 2voxilaprevir ethyl acetate
01 1South Korea
02 1Spain
Registrant Name : Gilead Sciences Korea Ltd.
Registration Date : 2022-03-23
Registration Number : Su205-25-ND
Manufacturer Name : Esteve Quimica, SA
Manufacturer Address : C/ Ter, 94 Polígon Industrial 17460 Celrà (Girona), Spain
Registrant Name : Gilead Sciences Korea Ltd.
Registration Date : 2022-03-23
Registration Number : 205-24-ND
Manufacturer Name : Yuhan Chemical Co., Ltd.
Manufacturer Address : 402, 5-ba, Sihwa Industrial Complex, 45 Jiwon-ro, Danwon-gu, Ansan-si, Gyeonggi-do (S...
A Voxilaprevir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Voxilaprevir, including repackagers and relabelers. The FDA regulates Voxilaprevir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Voxilaprevir 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 Voxilaprevir manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Voxilaprevir supplier is an individual or a company that provides Voxilaprevir active pharmaceutical ingredient (API) or Voxilaprevir finished formulations upon request. The Voxilaprevir suppliers may include Voxilaprevir API manufacturers, exporters, distributors and traders.
click here to find a list of Voxilaprevir suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price 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 Voxilaprevir Drug Master File in Korea (Voxilaprevir KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Voxilaprevir. The MFDS reviews the Voxilaprevir KDMF as part of the drug registration process and uses the information provided in the Voxilaprevir KDMF to evaluate the safety and efficacy of the drug.
After submitting a Voxilaprevir 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 Voxilaprevir API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Voxilaprevir suppliers with KDMF on PharmaCompass.
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