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