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