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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PharmaCompass also assists you with knowing the Vitamin B1 API Price utilized in the formulation of products. Vitamin B1 API Price is not always fixed or binding as the Vitamin B1 Price is obtained through a variety of data sources. The Vitamin B1 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A THIAMIN, VITAMIN B1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of THIAMIN, VITAMIN B1, including repackagers and relabelers. The FDA regulates THIAMIN, VITAMIN B1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. THIAMIN, VITAMIN B1 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 THIAMIN, VITAMIN B1 supplier is an individual or a company that provides THIAMIN, VITAMIN B1 active pharmaceutical ingredient (API) or THIAMIN, VITAMIN B1 finished formulations upon request. The THIAMIN, VITAMIN B1 suppliers may include THIAMIN, VITAMIN B1 API manufacturers, exporters, distributors and traders.
click here to find a list of THIAMIN, VITAMIN B1 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 THIAMIN, VITAMIN B1 Drug Master File in Japan (THIAMIN, VITAMIN B1 JDMF) empowers THIAMIN, VITAMIN B1 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 THIAMIN, VITAMIN B1 JDMF during the approval evaluation for pharmaceutical products. At the time of THIAMIN, VITAMIN B1 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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