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