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PharmaCompass offers a list of Flumequine 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 Flumequine manufacturer or Flumequine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Flumequine manufacturer or Flumequine supplier.
PharmaCompass also assists you with knowing the Flumequine API Price utilized in the formulation of products. Flumequine API Price is not always fixed or binding as the Flumequine Price is obtained through a variety of data sources. The Flumequine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Flumequine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flumequine, including repackagers and relabelers. The FDA regulates Flumequine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flumequine 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 Flumequine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Flumequine supplier is an individual or a company that provides Flumequine active pharmaceutical ingredient (API) or Flumequine finished formulations upon request. The Flumequine suppliers may include Flumequine API manufacturers, exporters, distributors and traders.
click here to find a list of Flumequine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Flumequine DMF (Drug Master File) is a document detailing the whole manufacturing process of Flumequine active pharmaceutical ingredient (API) in detail. Different forms of Flumequine DMFs exist exist since differing nations have different regulations, such as Flumequine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Flumequine DMF submitted to regulatory agencies in the US is known as a USDMF. Flumequine USDMF includes data on Flumequine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Flumequine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Flumequine suppliers with USDMF on PharmaCompass.
A Flumequine CEP of the European Pharmacopoeia monograph is often referred to as a Flumequine Certificate of Suitability (COS). The purpose of a Flumequine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Flumequine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Flumequine to their clients by showing that a Flumequine CEP has been issued for it. The manufacturer submits a Flumequine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Flumequine CEP holder for the record. Additionally, the data presented in the Flumequine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Flumequine DMF.
A Flumequine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Flumequine 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 Flumequine suppliers with CEP (COS) on PharmaCompass.
A Flumequine written confirmation (Flumequine WC) is an official document issued by a regulatory agency to a Flumequine manufacturer, verifying that the manufacturing facility of a Flumequine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Flumequine APIs or Flumequine finished pharmaceutical products to another nation, regulatory agencies frequently require a Flumequine WC (written confirmation) as part of the regulatory process.
click here to find a list of Flumequine suppliers with Written Confirmation (WC) on PharmaCompass.
Flumequine 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 Flumequine 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 Flumequine GMP manufacturer or Flumequine GMP API supplier for your needs.
A Flumequine CoA (Certificate of Analysis) is a formal document that attests to Flumequine's compliance with Flumequine specifications and serves as a tool for batch-level quality control.
Flumequine CoA mostly includes findings from lab analyses of a specific batch. For each Flumequine 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.
Flumequine may be tested according to a variety of international standards, such as European Pharmacopoeia (Flumequine EP), Flumequine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Flumequine USP).