01 1Taisho MTC Co., Ltd.
01 1Taurine
01 1Japan
Registration Number : 218MF10322
Registrant's Address : 1-5-2 Higashi-Shinbashi, Minato-ku, Tokyo
Initial Date of Registration : 2006-03-09
Latest Date of Registration : 2010-03-16
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PharmaCompass offers a list of Taurine 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 Taurine manufacturer or Taurine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Taurine manufacturer or Taurine supplier.
PharmaCompass also assists you with knowing the Taurine API Price utilized in the formulation of products. Taurine API Price is not always fixed or binding as the Taurine Price is obtained through a variety of data sources. The Taurine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Taurine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Taurine, including repackagers and relabelers. The FDA regulates Taurine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Taurine 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 Taurine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Taurine supplier is an individual or a company that provides Taurine active pharmaceutical ingredient (API) or Taurine finished formulations upon request. The Taurine suppliers may include Taurine API manufacturers, exporters, distributors and traders.
click here to find a list of Taurine 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 Taurine Drug Master File in Japan (Taurine JDMF) empowers Taurine 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 Taurine JDMF during the approval evaluation for pharmaceutical products. At the time of Taurine 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 Taurine suppliers with JDMF on PharmaCompass.
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