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ABOUT THIS PAGE
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PharmaCompass offers a list of Hexamidine 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 Hexamidine manufacturer or Hexamidine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hexamidine manufacturer or Hexamidine supplier.
PharmaCompass also assists you with knowing the Hexamidine API Price utilized in the formulation of products. Hexamidine API Price is not always fixed or binding as the Hexamidine Price is obtained through a variety of data sources. The Hexamidine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Desmedine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Desmedine, including repackagers and relabelers. The FDA regulates Desmedine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Desmedine 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 Desmedine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Desmedine supplier is an individual or a company that provides Desmedine active pharmaceutical ingredient (API) or Desmedine finished formulations upon request. The Desmedine suppliers may include Desmedine API manufacturers, exporters, distributors and traders.
click here to find a list of Desmedine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Desmedine CEP of the European Pharmacopoeia monograph is often referred to as a Desmedine Certificate of Suitability (COS). The purpose of a Desmedine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Desmedine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Desmedine to their clients by showing that a Desmedine CEP has been issued for it. The manufacturer submits a Desmedine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Desmedine CEP holder for the record. Additionally, the data presented in the Desmedine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Desmedine DMF.
A Desmedine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Desmedine CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Desmedine suppliers with CEP (COS) on PharmaCompass.
Desmedine 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 Desmedine 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 Desmedine GMP manufacturer or Desmedine GMP API supplier for your needs.
A Desmedine CoA (Certificate of Analysis) is a formal document that attests to Desmedine's compliance with Desmedine specifications and serves as a tool for batch-level quality control.
Desmedine CoA mostly includes findings from lab analyses of a specific batch. For each Desmedine 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.
Desmedine may be tested according to a variety of international standards, such as European Pharmacopoeia (Desmedine EP), Desmedine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Desmedine USP).
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