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