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
18
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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vitamin B1 manufacturer or Vitamin B1 supplier.
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 Thiamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Thiamine, including repackagers and relabelers. The FDA regulates Thiamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Thiamine 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 Thiamine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Thiamine supplier is an individual or a company that provides Thiamine active pharmaceutical ingredient (API) or Thiamine finished formulations upon request. The Thiamine suppliers may include Thiamine API manufacturers, exporters, distributors and traders.
click here to find a list of Thiamine 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 Thiamine Drug Master File in Japan (Thiamine JDMF) empowers Thiamine 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 Thiamine JDMF during the approval evaluation for pharmaceutical products. At the time of Thiamine 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 Thiamine suppliers with JDMF on PharmaCompass.
We have 1 companies offering Thiamine
Get in contact with the supplier of your choice:
