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