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PharmaCompass offers a list of Dasatinib 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 Dasatinib manufacturer or Dasatinib supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dasatinib manufacturer or Dasatinib supplier.
PharmaCompass also assists you with knowing the Dasatinib API Price utilized in the formulation of products. Dasatinib API Price is not always fixed or binding as the Dasatinib Price is obtained through a variety of data sources. The Dasatinib Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dasatinib anhydrous manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dasatinib anhydrous, including repackagers and relabelers. The FDA regulates Dasatinib anhydrous manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dasatinib anhydrous 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 Dasatinib anhydrous manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dasatinib anhydrous supplier is an individual or a company that provides Dasatinib anhydrous active pharmaceutical ingredient (API) or Dasatinib anhydrous finished formulations upon request. The Dasatinib anhydrous suppliers may include Dasatinib anhydrous API manufacturers, exporters, distributors and traders.
click here to find a list of Dasatinib anhydrous 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 Dasatinib anhydrous Drug Master File in Korea (Dasatinib anhydrous KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Dasatinib anhydrous. The MFDS reviews the Dasatinib anhydrous KDMF as part of the drug registration process and uses the information provided in the Dasatinib anhydrous KDMF to evaluate the safety and efficacy of the drug.
After submitting a Dasatinib anhydrous 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 Dasatinib anhydrous API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Dasatinib anhydrous suppliers with KDMF on PharmaCompass.
We have 5 companies offering Dasatinib anhydrous
Get in contact with the supplier of your choice: