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