01 1Kato Chemical Co., Ltd.
01 1Japanese Pharmacopoeia fructose (production only)
01 1Japan
Japanese Pharmacopoeia Fructose (for manufacturing purposes 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-Bisphosphate Sodium 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-Bisphosphate Sodium manufacturer or Fructose 1,6-Bisphosphate Sodium supplier for your needs.
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PharmaCompass also assists you with knowing the Fructose 1,6-Bisphosphate Sodium API Price utilized in the formulation of products. Fructose 1,6-Bisphosphate Sodium API Price is not always fixed or binding as the Fructose 1,6-Bisphosphate Sodium Price is obtained through a variety of data sources. The Fructose 1,6-Bisphosphate Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Fructose 1,6-Bisphosphate Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fructose 1,6-Bisphosphate Sodium, including repackagers and relabelers. The FDA regulates Fructose 1,6-Bisphosphate Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fructose 1,6-Bisphosphate Sodium 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-Bisphosphate Sodium supplier is an individual or a company that provides Fructose 1,6-Bisphosphate Sodium active pharmaceutical ingredient (API) or Fructose 1,6-Bisphosphate Sodium finished formulations upon request. The Fructose 1,6-Bisphosphate Sodium suppliers may include Fructose 1,6-Bisphosphate Sodium 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-Bisphosphate Sodium Drug Master File in Japan (Fructose 1,6-Bisphosphate Sodium JDMF) empowers Fructose 1,6-Bisphosphate Sodium 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-Bisphosphate Sodium JDMF during the approval evaluation for pharmaceutical products. At the time of Fructose 1,6-Bisphosphate Sodium 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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