01 1Hamari Pharmaceuticals Co., Ltd.
02 1Hetero Labs Limited
03 1Natco Pharma Limited.
04 1SUVEN LIFE SCIENCE LIMITED.
05 1Shin Poong Pharm. Co. , Ltd.
06 1Sumitomo Chemical Co., Ltd.
07 2TAPI Croatia Industries Ltd.
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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.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Gleevec Drug Master File in Japan (Gleevec JDMF) empowers Gleevec API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Gleevec JDMF during the approval evaluation for pharmaceutical products. At the time of Gleevec JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Gleevec suppliers with JDMF on PharmaCompass.
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