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ABOUT THIS PAGE
A Sulfogaiacol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sulfogaiacol, including repackagers and relabelers. The FDA regulates Sulfogaiacol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sulfogaiacol 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 Sulfogaiacol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sulfogaiacol supplier is an individual or a company that provides Sulfogaiacol active pharmaceutical ingredient (API) or Sulfogaiacol finished formulations upon request. The Sulfogaiacol suppliers may include Sulfogaiacol API manufacturers, exporters, distributors and traders.
click here to find a list of Sulfogaiacol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sulfogaiacol written confirmation (Sulfogaiacol WC) is an official document issued by a regulatory agency to a Sulfogaiacol manufacturer, verifying that the manufacturing facility of a Sulfogaiacol active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Sulfogaiacol APIs or Sulfogaiacol finished pharmaceutical products to another nation, regulatory agencies frequently require a Sulfogaiacol WC (written confirmation) as part of the regulatory process.
click here to find a list of Sulfogaiacol suppliers with Written Confirmation (WC) on PharmaCompass.
Sulfogaiacol 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 Sulfogaiacol 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 Sulfogaiacol GMP manufacturer or Sulfogaiacol GMP API supplier for your needs.
A Sulfogaiacol CoA (Certificate of Analysis) is a formal document that attests to Sulfogaiacol's compliance with Sulfogaiacol specifications and serves as a tool for batch-level quality control.
Sulfogaiacol CoA mostly includes findings from lab analyses of a specific batch. For each Sulfogaiacol 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.
Sulfogaiacol may be tested according to a variety of international standards, such as European Pharmacopoeia (Sulfogaiacol EP), Sulfogaiacol JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Sulfogaiacol USP).
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