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