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ABOUT THIS PAGE
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PharmaCompass offers a list of Gadolinium Ethoxybenzyl Dtpa 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 Gadolinium Ethoxybenzyl Dtpa manufacturer or Gadolinium Ethoxybenzyl Dtpa supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Gadolinium Ethoxybenzyl Dtpa manufacturer or Gadolinium Ethoxybenzyl Dtpa supplier.
PharmaCompass also assists you with knowing the Gadolinium Ethoxybenzyl Dtpa API Price utilized in the formulation of products. Gadolinium Ethoxybenzyl Dtpa API Price is not always fixed or binding as the Gadolinium Ethoxybenzyl Dtpa Price is obtained through a variety of data sources. The Gadolinium Ethoxybenzyl Dtpa Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A primovist manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of primovist, including repackagers and relabelers. The FDA regulates primovist manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. primovist 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 primovist manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A primovist supplier is an individual or a company that provides primovist active pharmaceutical ingredient (API) or primovist finished formulations upon request. The primovist suppliers may include primovist API manufacturers, exporters, distributors and traders.
click here to find a list of primovist suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A primovist DMF (Drug Master File) is a document detailing the whole manufacturing process of primovist active pharmaceutical ingredient (API) in detail. Different forms of primovist DMFs exist exist since differing nations have different regulations, such as primovist USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A primovist DMF submitted to regulatory agencies in the US is known as a USDMF. primovist USDMF includes data on primovist's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The primovist USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of primovist suppliers with USDMF on PharmaCompass.
A primovist written confirmation (primovist WC) is an official document issued by a regulatory agency to a primovist manufacturer, verifying that the manufacturing facility of a primovist active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting primovist APIs or primovist finished pharmaceutical products to another nation, regulatory agencies frequently require a primovist WC (written confirmation) as part of the regulatory process.
click here to find a list of primovist suppliers with Written Confirmation (WC) on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing primovist as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for primovist API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture primovist as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain primovist and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a primovist NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of primovist suppliers with NDC on PharmaCompass.
primovist 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 primovist 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 primovist GMP manufacturer or primovist GMP API supplier for your needs.
A primovist CoA (Certificate of Analysis) is a formal document that attests to primovist's compliance with primovist specifications and serves as a tool for batch-level quality control.
primovist CoA mostly includes findings from lab analyses of a specific batch. For each primovist 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.
primovist may be tested according to a variety of international standards, such as European Pharmacopoeia (primovist EP), primovist JP (Japanese Pharmacopeia) and the US Pharmacopoeia (primovist USP).
