01 1ICL ADVANCED ADDITIVES St Louis US
01 1Phosphoric acid, concentrated
01 1Israel
01 1Expired
Certificate Number : R0-CEP 2014-299 - Rev 01
Status : Expired
Issue Date : 2017-02-21
Type : Chemical
Substance Number : 4
99
PharmaCompass offers a list of Phosphoric Acid 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 Phosphoric Acid manufacturer or Phosphoric Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Phosphoric Acid manufacturer or Phosphoric Acid supplier.
PharmaCompass also assists you with knowing the Phosphoric Acid API Price utilized in the formulation of products. Phosphoric Acid API Price is not always fixed or binding as the Phosphoric Acid Price is obtained through a variety of data sources. The Phosphoric Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A H3PO4 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of H3PO4, including repackagers and relabelers. The FDA regulates H3PO4 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. H3PO4 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A H3PO4 supplier is an individual or a company that provides H3PO4 active pharmaceutical ingredient (API) or H3PO4 finished formulations upon request. The H3PO4 suppliers may include H3PO4 API manufacturers, exporters, distributors and traders.
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A H3PO4 CEP of the European Pharmacopoeia monograph is often referred to as a H3PO4 Certificate of Suitability (COS). The purpose of a H3PO4 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of H3PO4 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of H3PO4 to their clients by showing that a H3PO4 CEP has been issued for it. The manufacturer submits a H3PO4 CEP (COS) as part of the market authorization procedure, and it takes on the role of a H3PO4 CEP holder for the record. Additionally, the data presented in the H3PO4 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the H3PO4 DMF.
A H3PO4 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. H3PO4 CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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