01 1DEAD SEA BROMINE COMPANY LTD. Beer Sheva IL
01 1Magnesium oxide, heavy
01 1Israel
01 1Valid
Certificate Number : R1-CEP 2007-111 - Rev 02
Status : Valid
Issue Date : 2018-02-28
Type : Chemical
Substance Number : 41
57
PharmaCompass offers a list of Magnesium Oxide 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 Magnesium Oxide manufacturer or Magnesium Oxide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Magnesium Oxide manufacturer or Magnesium Oxide supplier.
PharmaCompass also assists you with knowing the Magnesium Oxide API Price utilized in the formulation of products. Magnesium Oxide API Price is not always fixed or binding as the Magnesium Oxide Price is obtained through a variety of data sources. The Magnesium Oxide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A E530 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of E530, including repackagers and relabelers. The FDA regulates E530 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. E530 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 E530 supplier is an individual or a company that provides E530 active pharmaceutical ingredient (API) or E530 finished formulations upon request. The E530 suppliers may include E530 API manufacturers, exporters, distributors and traders.
click here to find a list of E530 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A E530 CEP of the European Pharmacopoeia monograph is often referred to as a E530 Certificate of Suitability (COS). The purpose of a E530 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of E530 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of E530 to their clients by showing that a E530 CEP has been issued for it. The manufacturer submits a E530 CEP (COS) as part of the market authorization procedure, and it takes on the role of a E530 CEP holder for the record. Additionally, the data presented in the E530 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the E530 DMF.
A E530 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. E530 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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