01 1PETER GREVEN NEDERLAND C.V. Venlo NL
02 1PMC BIOGENIX, INC. Memphis US
03 1SO.G.I.S Industria Chimica SpA Sospiro IT
01 3Magnesium stearate
01 1Italy
02 1Netherlands
03 1U.S.A
01 3Valid
Certificate Number : CEP 2021-296 - Rev 00
Status : Valid
Issue Date : 2024-06-10
Type : Chemical
Substance Number : 229
Certificate Number : R1-CEP 2001-005 - Rev 01
Status : Valid
Issue Date : 2008-05-16
Type : TSE
Substance Number : 229
Certificate Number : R1-CEP 2001-039 - Rev 00
Status : Valid
Issue Date : 2006-11-02
Type : Chemical and TSE
Substance Number : 229
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PharmaCompass offers a list of Magnesium Stearate API 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 Stearate API manufacturer or Magnesium Stearate API supplier for your needs.
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PharmaCompass also assists you with knowing the Magnesium Stearate API API Price utilized in the formulation of products. Magnesium Stearate API API Price is not always fixed or binding as the Magnesium Stearate API Price is obtained through a variety of data sources. The Magnesium Stearate API Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Magnesium distearate, pure manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Magnesium distearate, pure, including repackagers and relabelers. The FDA regulates Magnesium distearate, pure manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Magnesium distearate, pure 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 Magnesium distearate, pure supplier is an individual or a company that provides Magnesium distearate, pure active pharmaceutical ingredient (API) or Magnesium distearate, pure finished formulations upon request. The Magnesium distearate, pure suppliers may include Magnesium distearate, pure API manufacturers, exporters, distributors and traders.
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A Magnesium distearate, pure CEP of the European Pharmacopoeia monograph is often referred to as a Magnesium distearate, pure Certificate of Suitability (COS). The purpose of a Magnesium distearate, pure CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Magnesium distearate, pure EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Magnesium distearate, pure to their clients by showing that a Magnesium distearate, pure CEP has been issued for it. The manufacturer submits a Magnesium distearate, pure CEP (COS) as part of the market authorization procedure, and it takes on the role of a Magnesium distearate, pure CEP holder for the record. Additionally, the data presented in the Magnesium distearate, pure CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Magnesium distearate, pure DMF.
A Magnesium distearate, pure CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Magnesium distearate, pure 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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