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PharmaCompass offers a list of Imatinib Mesylate 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 Imatinib Mesylate manufacturer or Imatinib Mesylate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Imatinib Mesylate manufacturer or Imatinib Mesylate supplier.
PharmaCompass also assists you with knowing the Imatinib Mesylate API Price utilized in the formulation of products. Imatinib Mesylate API Price is not always fixed or binding as the Imatinib Mesylate Price is obtained through a variety of data sources. The Imatinib Mesylate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Gleevec manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gleevec, including repackagers and relabelers. The FDA regulates Gleevec manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gleevec 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 Gleevec manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Gleevec supplier is an individual or a company that provides Gleevec active pharmaceutical ingredient (API) or Gleevec finished formulations upon request. The Gleevec suppliers may include Gleevec API manufacturers, exporters, distributors and traders.
click here to find a list of Gleevec suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Gleevec CEP of the European Pharmacopoeia monograph is often referred to as a Gleevec Certificate of Suitability (COS). The purpose of a Gleevec CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Gleevec EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Gleevec to their clients by showing that a Gleevec CEP has been issued for it. The manufacturer submits a Gleevec CEP (COS) as part of the market authorization procedure, and it takes on the role of a Gleevec CEP holder for the record. Additionally, the data presented in the Gleevec CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Gleevec DMF.
A Gleevec CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Gleevec CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Gleevec suppliers with CEP (COS) on PharmaCompass.
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