01 1B Food Science Co., Ltd.
02 1Mitsubishi Corporation Life Sciences Ltd.
01 1Japanese Pharmacopoeia xylitol
02 1Xylitol
01 2Japan
Japanese Pharmacopoeia Xylitol
Registration Number : 218MF10313
Registrant's Address : 24-12 Kitahamacho, Chita City, Aichi Prefecture
Initial Date of Registration : 2006-02-28
Latest Date of Registration : 2006-02-28
Registration Number : 217MF10326
Registrant's Address : 1-1-3 Yurakucho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2005-07-14
Latest Date of Registration : 2006-03-24
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PharmaCompass offers a list of Ribitol 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 Ribitol manufacturer or Ribitol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ribitol manufacturer or Ribitol supplier.
PharmaCompass also assists you with knowing the Ribitol API Price utilized in the formulation of products. Ribitol API Price is not always fixed or binding as the Ribitol Price is obtained through a variety of data sources. The Ribitol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A E967 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of E967, including repackagers and relabelers. The FDA regulates E967 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. E967 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 E967 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A E967 supplier is an individual or a company that provides E967 active pharmaceutical ingredient (API) or E967 finished formulations upon request. The E967 suppliers may include E967 API manufacturers, exporters, distributors and traders.
click here to find a list of E967 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 E967 Drug Master File in Japan (E967 JDMF) empowers E967 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 E967 JDMF during the approval evaluation for pharmaceutical products. At the time of E967 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 E967 suppliers with JDMF on PharmaCompass.
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