01 1Nagasevita Co., Ltd.
02 1Nippon Shokuhin Kako Co., Ltd.
03 1Sanas Co., Ltd.
01 2Japanese Pharmacopoeia maltose (production only)
02 1Solar eclipse crystalline maltose
01 3Japan
Japanese Pharmacopoeia Maltose (for manufacturing only)
Registration Number : 217MF10023
Registrant's Address : 675-1 Fujisaki, Naka-ku, Okayama City
Initial Date of Registration : 2005-05-18
Latest Date of Registration : 2010-02-17
Registration Number : 217MF10302
Registrant's Address : 1-6-5 Marunouchi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2005-06-30
Latest Date of Registration : 2005-12-15
Japanese Pharmacopoeia Maltose (for manufacturing only)
Registration Number : 218MF10588
Registrant's Address : 20 Minamiei 3-chome, Kagoshima City, Kagoshima Prefecture
Initial Date of Registration : 2006-06-22
Latest Date of Registration : 2006-06-22
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PharmaCompass offers a list of D-Maltose Monohydrate 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 D-Maltose Monohydrate manufacturer or D-Maltose Monohydrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred D-Maltose Monohydrate manufacturer or D-Maltose Monohydrate supplier.
PharmaCompass also assists you with knowing the D-Maltose Monohydrate API Price utilized in the formulation of products. D-Maltose Monohydrate API Price is not always fixed or binding as the D-Maltose Monohydrate Price is obtained through a variety of data sources. The D-Maltose Monohydrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A D-Maltose Monohydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of D-Maltose Monohydrate, including repackagers and relabelers. The FDA regulates D-Maltose Monohydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. D-Maltose Monohydrate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A D-Maltose Monohydrate supplier is an individual or a company that provides D-Maltose Monohydrate active pharmaceutical ingredient (API) or D-Maltose Monohydrate finished formulations upon request. The D-Maltose Monohydrate suppliers may include D-Maltose Monohydrate API manufacturers, exporters, distributors and traders.
click here to find a list of D-Maltose Monohydrate 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 D-Maltose Monohydrate Drug Master File in Japan (D-Maltose Monohydrate JDMF) empowers D-Maltose Monohydrate 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 D-Maltose Monohydrate JDMF during the approval evaluation for pharmaceutical products. At the time of D-Maltose Monohydrate 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 D-Maltose Monohydrate suppliers with JDMF on PharmaCompass.
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