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PharmaCompass offers a list of Cidofovir 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 Cidofovir manufacturer or Cidofovir supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cidofovir manufacturer or Cidofovir supplier.
PharmaCompass also assists you with knowing the Cidofovir API Price utilized in the formulation of products. Cidofovir API Price is not always fixed or binding as the Cidofovir Price is obtained through a variety of data sources. The Cidofovir Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cidofovir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cidofovir, including repackagers and relabelers. The FDA regulates Cidofovir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cidofovir 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 Cidofovir manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cidofovir supplier is an individual or a company that provides Cidofovir active pharmaceutical ingredient (API) or Cidofovir finished formulations upon request. The Cidofovir suppliers may include Cidofovir API manufacturers, exporters, distributors and traders.
click here to find a list of Cidofovir suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cidofovir DMF (Drug Master File) is a document detailing the whole manufacturing process of Cidofovir active pharmaceutical ingredient (API) in detail. Different forms of Cidofovir DMFs exist exist since differing nations have different regulations, such as Cidofovir USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cidofovir DMF submitted to regulatory agencies in the US is known as a USDMF. Cidofovir USDMF includes data on Cidofovir's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cidofovir USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Cidofovir suppliers with USDMF on PharmaCompass.
A Cidofovir written confirmation (Cidofovir WC) is an official document issued by a regulatory agency to a Cidofovir manufacturer, verifying that the manufacturing facility of a Cidofovir active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Cidofovir APIs or Cidofovir finished pharmaceutical products to another nation, regulatory agencies frequently require a Cidofovir WC (written confirmation) as part of the regulatory process.
click here to find a list of Cidofovir suppliers with Written Confirmation (WC) on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Cidofovir as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Cidofovir API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Cidofovir as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Cidofovir and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cidofovir NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Cidofovir suppliers with NDC on PharmaCompass.
Cidofovir 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 Cidofovir 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 Cidofovir GMP manufacturer or Cidofovir GMP API supplier for your needs.
A Cidofovir CoA (Certificate of Analysis) is a formal document that attests to Cidofovir's compliance with Cidofovir specifications and serves as a tool for batch-level quality control.
Cidofovir CoA mostly includes findings from lab analyses of a specific batch. For each Cidofovir 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.
Cidofovir may be tested according to a variety of international standards, such as European Pharmacopoeia (Cidofovir EP), Cidofovir JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Cidofovir USP).
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