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.
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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 UN1805 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of UN1805, including repackagers and relabelers. The FDA regulates UN1805 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. UN1805 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 UN1805 supplier is an individual or a company that provides UN1805 active pharmaceutical ingredient (API) or UN1805 finished formulations upon request. The UN1805 suppliers may include UN1805 API manufacturers, exporters, distributors and traders.
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A UN1805 CEP of the European Pharmacopoeia monograph is often referred to as a UN1805 Certificate of Suitability (COS). The purpose of a UN1805 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of UN1805 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of UN1805 to their clients by showing that a UN1805 CEP has been issued for it. The manufacturer submits a UN1805 CEP (COS) as part of the market authorization procedure, and it takes on the role of a UN1805 CEP holder for the record. Additionally, the data presented in the UN1805 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the UN1805 DMF.
A UN1805 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. UN1805 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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