Synopsis
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
EDQM
0
USP
0
JP
0
Others
0
FDF Dossiers
0
FDA Orange Book
0
Europe
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
US Patents
0
US Exclusivities
0
Health Canada Patents
US Medicaid
NA
Annual Reports
NA
Regulatory FDF Prices
NA
0
API
0
FDF
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
API SUPPLIERS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
USDMF
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Listed Suppliers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]API Reference Price
API/FDF Prices: Book a Demo to explore the features and consider upgrading later
API Imports and Exports
ABOUT THIS PAGE
90
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 SODIUM [JAN] manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DIQUAFOSOL SODIUM [JAN], including repackagers and relabelers. The FDA regulates DIQUAFOSOL SODIUM [JAN] manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DIQUAFOSOL SODIUM [JAN] 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 SODIUM [JAN] manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DIQUAFOSOL SODIUM [JAN] supplier is an individual or a company that provides DIQUAFOSOL SODIUM [JAN] active pharmaceutical ingredient (API) or DIQUAFOSOL SODIUM [JAN] finished formulations upon request. The DIQUAFOSOL SODIUM [JAN] suppliers may include DIQUAFOSOL SODIUM [JAN] API manufacturers, exporters, distributors and traders.
click here to find a list of DIQUAFOSOL SODIUM [JAN] suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DIQUAFOSOL SODIUM [JAN] DMF (Drug Master File) is a document detailing the whole manufacturing process of DIQUAFOSOL SODIUM [JAN] active pharmaceutical ingredient (API) in detail. Different forms of DIQUAFOSOL SODIUM [JAN] DMFs exist exist since differing nations have different regulations, such as DIQUAFOSOL SODIUM [JAN] USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A DIQUAFOSOL SODIUM [JAN] DMF submitted to regulatory agencies in the US is known as a USDMF. DIQUAFOSOL SODIUM [JAN] USDMF includes data on DIQUAFOSOL SODIUM [JAN]'s chemical properties, information on the facilities and procedures used, and details about packaging and storage. The DIQUAFOSOL SODIUM [JAN] USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of DIQUAFOSOL SODIUM [JAN] suppliers with USDMF on PharmaCompass.
DIQUAFOSOL SODIUM [JAN] 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 SODIUM [JAN] 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 SODIUM [JAN] GMP manufacturer or DIQUAFOSOL SODIUM [JAN] GMP API supplier for your needs.
A DIQUAFOSOL SODIUM [JAN] CoA (Certificate of Analysis) is a formal document that attests to DIQUAFOSOL SODIUM [JAN]'s compliance with DIQUAFOSOL SODIUM [JAN] specifications and serves as a tool for batch-level quality control.
DIQUAFOSOL SODIUM [JAN] CoA mostly includes findings from lab analyses of a specific batch. For each DIQUAFOSOL SODIUM [JAN] 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 SODIUM [JAN] may be tested according to a variety of international standards, such as European Pharmacopoeia (DIQUAFOSOL SODIUM [JAN] EP), DIQUAFOSOL SODIUM [JAN] JP (Japanese Pharmacopeia) and the US Pharmacopoeia (DIQUAFOSOL SODIUM [JAN] USP).
