01 1Kato Chemicals Co., Ltd.
01 1Japanese Pharmacopoeia fructose (production only)
01 1Japan
Japanese Pharmacopoeia Fructose (for manufacturing only)
Registration Number : 218MF10358
Registrant's Address : 18 Kamimaeda, Kawawa, Mihama-cho, Chita-gun, Aichi Prefecture
Initial Date of Registration : 2006-03-17
Latest Date of Registration : 2006-03-17
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PharmaCompass offers a list of Fructose-1,6-Diphosphate 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 Fructose-1,6-Diphosphate manufacturer or Fructose-1,6-Diphosphate supplier for your needs.
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PharmaCompass also assists you with knowing the Fructose-1,6-Diphosphate API Price utilized in the formulation of products. Fructose-1,6-Diphosphate API Price is not always fixed or binding as the Fructose-1,6-Diphosphate Price is obtained through a variety of data sources. The Fructose-1,6-Diphosphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A fructose-1,6-diphosphate magnesium salt manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of fructose-1,6-diphosphate magnesium salt, including repackagers and relabelers. The FDA regulates fructose-1,6-diphosphate magnesium salt manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. fructose-1,6-diphosphate magnesium salt API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A fructose-1,6-diphosphate magnesium salt supplier is an individual or a company that provides fructose-1,6-diphosphate magnesium salt active pharmaceutical ingredient (API) or fructose-1,6-diphosphate magnesium salt finished formulations upon request. The fructose-1,6-diphosphate magnesium salt suppliers may include fructose-1,6-diphosphate magnesium salt API manufacturers, exporters, distributors and traders.
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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 fructose-1,6-diphosphate magnesium salt Drug Master File in Japan (fructose-1,6-diphosphate magnesium salt JDMF) empowers fructose-1,6-diphosphate magnesium salt 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 fructose-1,6-diphosphate magnesium salt JDMF during the approval evaluation for pharmaceutical products. At the time of fructose-1,6-diphosphate magnesium salt JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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