API Suppliers
US DMFs Filed
0
CEP/COS Certifications
0
JDMFs Filed
Other Certificates
0
Other Suppliers
0
USA (Orange Book)
Europe
Canada
0
Australia
South Africa
Uploaded Dossiers
U.S. Medicaid
0
Annual Reports
0
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.
Thiamine Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of Thiamine GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Thiamine GMP manufacturer or Thiamine GMP API supplier for your needs.
A Thiamine CoA (Certificate of Analysis) is a formal document that attests to Thiamine's compliance with Thiamine specifications and serves as a tool for batch-level quality control.
Thiamine CoA mostly includes findings from lab analyses of a specific batch. For each Thiamine CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
Thiamine may be tested according to a variety of international standards, such as European Pharmacopoeia (Thiamine EP), Thiamine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Thiamine USP).