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Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Switzerland
Anhydrous glucose; sodium chloride; potassium chloride; sodium citrate dihydrate
Brand Name : Elotrans
Dosage Form : Plv
Dosage Strength :
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
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PharmaCompass offers a list of Sodium Citrate 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 Sodium Citrate manufacturer or Sodium Citrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Citrate manufacturer or Sodium Citrate supplier.
PharmaCompass also assists you with knowing the Sodium Citrate API Price utilized in the formulation of products. Sodium Citrate API Price is not always fixed or binding as the Sodium Citrate Price is obtained through a variety of data sources. The Sodium Citrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Natrocitral manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Natrocitral, including repackagers and relabelers. The FDA regulates Natrocitral manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Natrocitral 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 Natrocitral manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Natrocitral supplier is an individual or a company that provides Natrocitral active pharmaceutical ingredient (API) or Natrocitral finished formulations upon request. The Natrocitral suppliers may include Natrocitral API manufacturers, exporters, distributors and traders.
click here to find a list of Natrocitral suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Natrocitral DMF (Drug Master File) is a document detailing the whole manufacturing process of Natrocitral active pharmaceutical ingredient (API) in detail. Different forms of Natrocitral DMFs exist exist since differing nations have different regulations, such as Natrocitral USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Natrocitral DMF submitted to regulatory agencies in the US is known as a USDMF. Natrocitral USDMF includes data on Natrocitral's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Natrocitral USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Natrocitral suppliers with USDMF on PharmaCompass.
A Natrocitral CEP of the European Pharmacopoeia monograph is often referred to as a Natrocitral Certificate of Suitability (COS). The purpose of a Natrocitral CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Natrocitral EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Natrocitral to their clients by showing that a Natrocitral CEP has been issued for it. The manufacturer submits a Natrocitral CEP (COS) as part of the market authorization procedure, and it takes on the role of a Natrocitral CEP holder for the record. Additionally, the data presented in the Natrocitral CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Natrocitral DMF.
A Natrocitral CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Natrocitral CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Natrocitral suppliers with CEP (COS) on PharmaCompass.
Natrocitral 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 Natrocitral 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 Natrocitral GMP manufacturer or Natrocitral GMP API supplier for your needs.
A Natrocitral CoA (Certificate of Analysis) is a formal document that attests to Natrocitral's compliance with Natrocitral specifications and serves as a tool for batch-level quality control.
Natrocitral CoA mostly includes findings from lab analyses of a specific batch. For each Natrocitral 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.
Natrocitral may be tested according to a variety of international standards, such as European Pharmacopoeia (Natrocitral EP), Natrocitral JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Natrocitral USP).
