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