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01 Active Pharma Co., Ltd. (1)
02 Chugoku Kayaku Co., Ltd. (1)
03 Hamari PFST Co., Ltd. (2)
04 Kanto Chemical Co., Ltd. (1)
05 Sanyo Chemical Research Institute Co., Ltd. (1)
06 Shionogi Pharma Co., Ltd. (1)
01 Edaravone (7)
01 Gabon (1)
02 Japan (6)
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PharmaCompass offers a list of Edaravone 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 Edaravone manufacturer or Edaravone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Edaravone manufacturer or Edaravone supplier.
PharmaCompass also assists you with knowing the Edaravone API Price utilized in the formulation of products. Edaravone API Price is not always fixed or binding as the Edaravone Price is obtained through a variety of data sources. The Edaravone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AM20060748 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AM20060748, including repackagers and relabelers. The FDA regulates AM20060748 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AM20060748 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 AM20060748 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A AM20060748 supplier is an individual or a company that provides AM20060748 active pharmaceutical ingredient (API) or AM20060748 finished formulations upon request. The AM20060748 suppliers may include AM20060748 API manufacturers, exporters, distributors and traders.
click here to find a list of AM20060748 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 AM20060748 Drug Master File in Japan (AM20060748 JDMF) empowers AM20060748 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 AM20060748 JDMF during the approval evaluation for pharmaceutical products. At the time of AM20060748 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 AM20060748 suppliers with JDMF on PharmaCompass.
We have 6 companies offering AM20060748
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