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01 1DEAD SEA BROMINE COMPANY LTD. Beer Sheva IL
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01 1Magnesium oxide, heavy
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01 1Israel
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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 Luvatol MK 35 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Luvatol MK 35, including repackagers and relabelers. The FDA regulates Luvatol MK 35 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Luvatol MK 35 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 Luvatol MK 35 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Luvatol MK 35 supplier is an individual or a company that provides Luvatol MK 35 active pharmaceutical ingredient (API) or Luvatol MK 35 finished formulations upon request. The Luvatol MK 35 suppliers may include Luvatol MK 35 API manufacturers, exporters, distributors and traders.
click here to find a list of Luvatol MK 35 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Luvatol MK 35 CEP of the European Pharmacopoeia monograph is often referred to as a Luvatol MK 35 Certificate of Suitability (COS). The purpose of a Luvatol MK 35 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Luvatol MK 35 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Luvatol MK 35 to their clients by showing that a Luvatol MK 35 CEP has been issued for it. The manufacturer submits a Luvatol MK 35 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Luvatol MK 35 CEP holder for the record. Additionally, the data presented in the Luvatol MK 35 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Luvatol MK 35 DMF.
A Luvatol MK 35 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Luvatol MK 35 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 Luvatol MK 35 suppliers with CEP (COS) on PharmaCompass.
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