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
25
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 Hyflo Super Cel medium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hyflo Super Cel medium, including repackagers and relabelers. The FDA regulates Hyflo Super Cel medium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hyflo Super Cel medium 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 Hyflo Super Cel medium supplier is an individual or a company that provides Hyflo Super Cel medium active pharmaceutical ingredient (API) or Hyflo Super Cel medium finished formulations upon request. The Hyflo Super Cel medium suppliers may include Hyflo Super Cel medium API manufacturers, exporters, distributors and traders.
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A Hyflo Super Cel medium CEP of the European Pharmacopoeia monograph is often referred to as a Hyflo Super Cel medium Certificate of Suitability (COS). The purpose of a Hyflo Super Cel medium CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Hyflo Super Cel medium EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Hyflo Super Cel medium to their clients by showing that a Hyflo Super Cel medium CEP has been issued for it. The manufacturer submits a Hyflo Super Cel medium CEP (COS) as part of the market authorization procedure, and it takes on the role of a Hyflo Super Cel medium CEP holder for the record. Additionally, the data presented in the Hyflo Super Cel medium CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Hyflo Super Cel medium DMF.
A Hyflo Super Cel medium CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Hyflo Super Cel medium 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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