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PharmaCompass offers a list of Endotoxin 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 Endotoxin manufacturer or Endotoxin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Endotoxin manufacturer or Endotoxin supplier.
PharmaCompass also assists you with knowing the Endotoxin API Price utilized in the formulation of products. Endotoxin API Price is not always fixed or binding as the Endotoxin Price is obtained through a variety of data sources. The Endotoxin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Endotoxin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Endotoxin, including repackagers and relabelers. The FDA regulates Endotoxin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Endotoxin API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Endotoxin supplier is an individual or a company that provides Endotoxin active pharmaceutical ingredient (API) or Endotoxin finished formulations upon request. The Endotoxin suppliers may include Endotoxin API manufacturers, exporters, distributors and traders.
Endotoxin 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 Endotoxin 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 Endotoxin GMP manufacturer or Endotoxin GMP API supplier for your needs.
A Endotoxin CoA (Certificate of Analysis) is a formal document that attests to Endotoxin's compliance with Endotoxin specifications and serves as a tool for batch-level quality control.
Endotoxin CoA mostly includes findings from lab analyses of a specific batch. For each Endotoxin 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.
Endotoxin may be tested according to a variety of international standards, such as European Pharmacopoeia (Endotoxin EP), Endotoxin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Endotoxin USP).