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