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