01 1TRUTAG TECHNOLOGIES, INC. Kapolei US
01 1Silica, colloidal anhydrous
01 1U.S.A
01 1Valid
Certificate Number : R0-CEP 2020-282 - Rev 00
Status : Valid
Issue Date : 2022-10-03
Type : Chemical
Substance Number : 434
71
PharmaCompass offers a list of Silicon Dioxide 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 Silicon Dioxide API manufacturer or Silicon Dioxide API supplier for your needs.
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PharmaCompass also assists you with knowing the Silicon Dioxide API API Price utilized in the formulation of products. Silicon Dioxide API API Price is not always fixed or binding as the Silicon Dioxide API Price is obtained through a variety of data sources. The Silicon Dioxide API Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Colloidal silicon dioxide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Colloidal silicon dioxide, including repackagers and relabelers. The FDA regulates Colloidal silicon dioxide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Colloidal silicon dioxide 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 Colloidal silicon dioxide supplier is an individual or a company that provides Colloidal silicon dioxide active pharmaceutical ingredient (API) or Colloidal silicon dioxide finished formulations upon request. The Colloidal silicon dioxide suppliers may include Colloidal silicon dioxide API manufacturers, exporters, distributors and traders.
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A Colloidal silicon dioxide CEP of the European Pharmacopoeia monograph is often referred to as a Colloidal silicon dioxide Certificate of Suitability (COS). The purpose of a Colloidal silicon dioxide CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Colloidal silicon dioxide EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Colloidal silicon dioxide to their clients by showing that a Colloidal silicon dioxide CEP has been issued for it. The manufacturer submits a Colloidal silicon dioxide CEP (COS) as part of the market authorization procedure, and it takes on the role of a Colloidal silicon dioxide CEP holder for the record. Additionally, the data presented in the Colloidal silicon dioxide CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Colloidal silicon dioxide DMF.
A Colloidal silicon dioxide CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Colloidal silicon dioxide 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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