01 1MSD International GmbH
01 1Korea MSD Co., Ltd.
01 1Boceprevir
01 1U.S.A
Registrant Name : Korea MSD Co., Ltd.
Registration Date : 2014-06-24
Registration Number : Su3281-14-ND
Manufacturer Name : MSD International GmbH
Manufacturer Address : 50 Tuas West Drive Singapore 638408
100
PharmaCompass offers a list of Boceprevir API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Boceprevir manufacturer or Boceprevir supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Boceprevir manufacturer or Boceprevir supplier.
PharmaCompass also assists you with knowing the Boceprevir API Price utilized in the formulation of products. Boceprevir API Price is not always fixed or binding as the Boceprevir Price is obtained through a variety of data sources. The Boceprevir Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Victrelis (TN) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Victrelis (TN), including repackagers and relabelers. The FDA regulates Victrelis (TN) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Victrelis (TN) API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Victrelis (TN) supplier is an individual or a company that provides Victrelis (TN) active pharmaceutical ingredient (API) or Victrelis (TN) finished formulations upon request. The Victrelis (TN) suppliers may include Victrelis (TN) API manufacturers, exporters, distributors and traders.
click here to find a list of Victrelis (TN) 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 Victrelis (TN) Drug Master File in Korea (Victrelis (TN) KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Victrelis (TN). The MFDS reviews the Victrelis (TN) KDMF as part of the drug registration process and uses the information provided in the Victrelis (TN) KDMF to evaluate the safety and efficacy of the drug.
After submitting a Victrelis (TN) 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 Victrelis (TN) API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Victrelis (TN) suppliers with KDMF on PharmaCompass.
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