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