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