01 1Osaka Synthetic Organic Chemical Research Institute, Inc.
01 1Deferasirox manufacturing only
01 1Japan
Deferasirox Manufacturing Only
Registration Number : 231MF10012
Registrant's Address : 1-1-2 Nishinomiyahama, Nishinomiya City, Hyogo Prefecture
Initial Date of Registration : 2019-01-11
Latest Date of Registration : 2021-05-17
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PharmaCompass offers a list of Deferasirox 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 Deferasirox manufacturer or Deferasirox supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Deferasirox manufacturer or Deferasirox supplier.
PharmaCompass also assists you with knowing the Deferasirox API Price utilized in the formulation of products. Deferasirox API Price is not always fixed or binding as the Deferasirox Price is obtained through a variety of data sources. The Deferasirox Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Exjade manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Exjade, including repackagers and relabelers. The FDA regulates Exjade manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Exjade 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 Exjade manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Exjade supplier is an individual or a company that provides Exjade active pharmaceutical ingredient (API) or Exjade finished formulations upon request. The Exjade suppliers may include Exjade API manufacturers, exporters, distributors and traders.
click here to find a list of Exjade 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 Exjade Drug Master File in Japan (Exjade JDMF) empowers Exjade 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 Exjade JDMF during the approval evaluation for pharmaceutical products. At the time of Exjade 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 Exjade suppliers with JDMF on PharmaCompass.
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