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