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