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
62
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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Fluoride manufacturer or Sodium Fluoride supplier.
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 Cavi-trol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cavi-trol, including repackagers and relabelers. The FDA regulates Cavi-trol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cavi-trol 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 Cavi-trol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cavi-trol supplier is an individual or a company that provides Cavi-trol active pharmaceutical ingredient (API) or Cavi-trol finished formulations upon request. The Cavi-trol suppliers may include Cavi-trol API manufacturers, exporters, distributors and traders.
click here to find a list of Cavi-trol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cavi-trol CEP of the European Pharmacopoeia monograph is often referred to as a Cavi-trol Certificate of Suitability (COS). The purpose of a Cavi-trol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cavi-trol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cavi-trol to their clients by showing that a Cavi-trol CEP has been issued for it. The manufacturer submits a Cavi-trol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cavi-trol CEP holder for the record. Additionally, the data presented in the Cavi-trol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cavi-trol DMF.
A Cavi-trol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cavi-trol 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 Cavi-trol suppliers with CEP (COS) on PharmaCompass.
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