01 2Mingtai Chemical Co., Ltd. Taoyuan Hsien TW
01 1Croscarmellose sodium
02 1Croscarmellose sodium, Process II
01 2China
01 2Valid
Croscarmellose Sodium, Process II
Certificate Number : R1-CEP 2012-141 - Rev 00
Status : Valid
Issue Date : 2019-09-18
Type : Chemical
Substance Number : 985
Certificate Number : R1-CEP 2002-250 - Rev 00
Status : Valid
Issue Date : 2010-02-24
Type : Chemical
Substance Number : 985
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PharmaCompass offers a list of Sodium Carboxymethylcellulose 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 Sodium Carboxymethylcellulose manufacturer or Sodium Carboxymethylcellulose supplier for your needs.
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A Cellufix FF 100 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cellufix FF 100, including repackagers and relabelers. The FDA regulates Cellufix FF 100 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cellufix FF 100 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 Cellufix FF 100 supplier is an individual or a company that provides Cellufix FF 100 active pharmaceutical ingredient (API) or Cellufix FF 100 finished formulations upon request. The Cellufix FF 100 suppliers may include Cellufix FF 100 API manufacturers, exporters, distributors and traders.
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A Cellufix FF 100 CEP of the European Pharmacopoeia monograph is often referred to as a Cellufix FF 100 Certificate of Suitability (COS). The purpose of a Cellufix FF 100 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cellufix FF 100 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cellufix FF 100 to their clients by showing that a Cellufix FF 100 CEP has been issued for it. The manufacturer submits a Cellufix FF 100 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cellufix FF 100 CEP holder for the record. Additionally, the data presented in the Cellufix FF 100 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cellufix FF 100 DMF.
A Cellufix FF 100 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cellufix FF 100 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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