01 1Bussan Food Science Co., Ltd.
01 1Japanese Pharmacopoeia D- mannitol
01 1Japan
Japanese Pharmacopoeia D-Mannitol
Registration Number : 218MF10311
Registrant's Address : 24-12 Kitahamacho, Chita City, Aichi Prefecture
Initial Date of Registration : 2006-02-28
Latest Date of Registration : 2006-02-28
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PharmaCompass offers a list of Mannitol API 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 Mannitol API manufacturer or Mannitol API supplier for your needs.
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PharmaCompass also assists you with knowing the Mannitol API API Price utilized in the formulation of products. Mannitol API API Price is not always fixed or binding as the Mannitol API Price is obtained through a variety of data sources. The Mannitol API Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A (2R,3R,4R,5R)-hexane-1,2,3,4,5,6-hexol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (2R,3R,4R,5R)-hexane-1,2,3,4,5,6-hexol, including repackagers and relabelers. The FDA regulates (2R,3R,4R,5R)-hexane-1,2,3,4,5,6-hexol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (2R,3R,4R,5R)-hexane-1,2,3,4,5,6-hexol 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 (2R,3R,4R,5R)-hexane-1,2,3,4,5,6-hexol supplier is an individual or a company that provides (2R,3R,4R,5R)-hexane-1,2,3,4,5,6-hexol active pharmaceutical ingredient (API) or (2R,3R,4R,5R)-hexane-1,2,3,4,5,6-hexol finished formulations upon request. The (2R,3R,4R,5R)-hexane-1,2,3,4,5,6-hexol suppliers may include (2R,3R,4R,5R)-hexane-1,2,3,4,5,6-hexol 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 (2R,3R,4R,5R)-hexane-1,2,3,4,5,6-hexol Drug Master File in Japan ((2R,3R,4R,5R)-hexane-1,2,3,4,5,6-hexol JDMF) empowers (2R,3R,4R,5R)-hexane-1,2,3,4,5,6-hexol 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 (2R,3R,4R,5R)-hexane-1,2,3,4,5,6-hexol JDMF during the approval evaluation for pharmaceutical products. At the time of (2R,3R,4R,5R)-hexane-1,2,3,4,5,6-hexol 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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We have 1 companies offering (2R,3R,4R,5R)-hexane-1,2,3,4,5,6-hexol
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