01 1Tsuno Rice Fine Chemicals Co., Ltd.
01 1Inositol
01 1Japan
Registration Number : 218MF10856
Registrant's Address : 2283 Chonomachi, Katsuragi-cho, Ito-gun, Wakayama Prefecture
Initial Date of Registration : 2006-11-06
Latest Date of Registration : 2007-07-26
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PharmaCompass offers a list of Inositol 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 Inositol manufacturer or Inositol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Inositol manufacturer or Inositol supplier.
PharmaCompass also assists you with knowing the Inositol API Price utilized in the formulation of products. Inositol API Price is not always fixed or binding as the Inositol Price is obtained through a variety of data sources. The Inositol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CBU manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CBU, including repackagers and relabelers. The FDA regulates CBU manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CBU 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 CBU manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CBU supplier is an individual or a company that provides CBU active pharmaceutical ingredient (API) or CBU finished formulations upon request. The CBU suppliers may include CBU API manufacturers, exporters, distributors and traders.
click here to find a list of CBU 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 CBU Drug Master File in Japan (CBU JDMF) empowers CBU 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 CBU JDMF during the approval evaluation for pharmaceutical products. At the time of CBU 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 CBU suppliers with JDMF on PharmaCompass.
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