01 1Merck KGaA Darmstadt DE
02 1QUALITY CHEMICALS S.L. Esparreguera ES
01 2Sodium fluoride
01 1Germany
02 1Spain
01 2Valid
Certificate Number : R1-CEP 1997-088 - Rev 04
Status : Valid
Issue Date : 2018-01-11
Type : Chemical
Substance Number : 514
Certificate Number : R1-CEP 2016-103 - Rev 00
Status : Valid
Issue Date : 2022-03-18
Type : Chemical
Substance Number : 514
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PharmaCompass offers a list of Sodium Fluoride 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 Sodium Fluoride manufacturer or Sodium Fluoride supplier for your needs.
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PharmaCompass also assists you with knowing the Sodium Fluoride API Price utilized in the formulation of products. Sodium Fluoride API Price is not always fixed or binding as the Sodium Fluoride Price is obtained through a variety of data sources. The Sodium Fluoride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Luride lozi-tabs manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Luride lozi-tabs, including repackagers and relabelers. The FDA regulates Luride lozi-tabs manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Luride lozi-tabs 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 Luride lozi-tabs supplier is an individual or a company that provides Luride lozi-tabs active pharmaceutical ingredient (API) or Luride lozi-tabs finished formulations upon request. The Luride lozi-tabs suppliers may include Luride lozi-tabs API manufacturers, exporters, distributors and traders.
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A Luride lozi-tabs CEP of the European Pharmacopoeia monograph is often referred to as a Luride lozi-tabs Certificate of Suitability (COS). The purpose of a Luride lozi-tabs CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Luride lozi-tabs EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Luride lozi-tabs to their clients by showing that a Luride lozi-tabs CEP has been issued for it. The manufacturer submits a Luride lozi-tabs CEP (COS) as part of the market authorization procedure, and it takes on the role of a Luride lozi-tabs CEP holder for the record. Additionally, the data presented in the Luride lozi-tabs CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Luride lozi-tabs DMF.
A Luride lozi-tabs CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Luride lozi-tabs 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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