01 1Tateyama Chemical Co., Ltd.
01 1Oct thiamine (Tateyama
01 1Japan
Registration Number : 217MF10337
Registrant's Address : 1133 Oe, Imizu City, Toyama Prefecture
Initial Date of Registration : 2005-07-21
Latest Date of Registration : 2010-03-23
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PharmaCompass offers a list of Vitamin B1 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 Vitamin B1 manufacturer or Vitamin B1 supplier for your needs.
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A Bevitex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bevitex, including repackagers and relabelers. The FDA regulates Bevitex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bevitex 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 Bevitex supplier is an individual or a company that provides Bevitex active pharmaceutical ingredient (API) or Bevitex finished formulations upon request. The Bevitex suppliers may include Bevitex API manufacturers, exporters, distributors and traders.
click here to find a list of Bevitex 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 Bevitex Drug Master File in Japan (Bevitex JDMF) empowers Bevitex 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 Bevitex JDMF during the approval evaluation for pharmaceutical products. At the time of Bevitex 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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