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