01 CFL CHEMISCHE FABRIK LEHRTE GMBH & CO. KG Lehrte DE (1)
02 MACCO ORGANIQUES, S.R.O. Bruntál CZ (1)
03 Merck KGaA Darmstadt DE (1)
01 Magnesium chloride hexahydrate (3)
01 Czech Republic (1)
02 Germany (2)
01 Valid (3)
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PharmaCompass offers a list of Magnesium Chloride 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 Chloride manufacturer or Magnesium Chloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Magnesium Chloride manufacturer or Magnesium Chloride supplier.
PharmaCompass also assists you with knowing the Magnesium Chloride API Price utilized in the formulation of products. Magnesium Chloride API Price is not always fixed or binding as the Magnesium Chloride Price is obtained through a variety of data sources. The Magnesium Chloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 02F3473H9O manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 02F3473H9O, including repackagers and relabelers. The FDA regulates 02F3473H9O manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 02F3473H9O 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 02F3473H9O supplier is an individual or a company that provides 02F3473H9O active pharmaceutical ingredient (API) or 02F3473H9O finished formulations upon request. The 02F3473H9O suppliers may include 02F3473H9O API manufacturers, exporters, distributors and traders.
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A 02F3473H9O CEP of the European Pharmacopoeia monograph is often referred to as a 02F3473H9O Certificate of Suitability (COS). The purpose of a 02F3473H9O CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 02F3473H9O EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 02F3473H9O to their clients by showing that a 02F3473H9O CEP has been issued for it. The manufacturer submits a 02F3473H9O CEP (COS) as part of the market authorization procedure, and it takes on the role of a 02F3473H9O CEP holder for the record. Additionally, the data presented in the 02F3473H9O CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 02F3473H9O DMF.
A 02F3473H9O CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 02F3473H9O 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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