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.
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A (2R,4S)-pentane-1,2,3,4,5-pentol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (2R,4S)-pentane-1,2,3,4,5-pentol, including repackagers and relabelers. The FDA regulates (2R,4S)-pentane-1,2,3,4,5-pentol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (2R,4S)-pentane-1,2,3,4,5-pentol 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,4S)-pentane-1,2,3,4,5-pentol supplier is an individual or a company that provides (2R,4S)-pentane-1,2,3,4,5-pentol active pharmaceutical ingredient (API) or (2R,4S)-pentane-1,2,3,4,5-pentol finished formulations upon request. The (2R,4S)-pentane-1,2,3,4,5-pentol suppliers may include (2R,4S)-pentane-1,2,3,4,5-pentol 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,4S)-pentane-1,2,3,4,5-pentol Drug Master File in Japan ((2R,4S)-pentane-1,2,3,4,5-pentol JDMF) empowers (2R,4S)-pentane-1,2,3,4,5-pentol 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,4S)-pentane-1,2,3,4,5-pentol JDMF during the approval evaluation for pharmaceutical products. At the time of (2R,4S)-pentane-1,2,3,4,5-pentol 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 2 companies offering (2R,4S)-pentane-1,2,3,4,5-pentol
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