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