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 Tylose C 300 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tylose C 300, including repackagers and relabelers. The FDA regulates Tylose C 300 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tylose C 300 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 Tylose C 300 supplier is an individual or a company that provides Tylose C 300 active pharmaceutical ingredient (API) or Tylose C 300 finished formulations upon request. The Tylose C 300 suppliers may include Tylose C 300 API manufacturers, exporters, distributors and traders.
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A Tylose C 300 CEP of the European Pharmacopoeia monograph is often referred to as a Tylose C 300 Certificate of Suitability (COS). The purpose of a Tylose C 300 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tylose C 300 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tylose C 300 to their clients by showing that a Tylose C 300 CEP has been issued for it. The manufacturer submits a Tylose C 300 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tylose C 300 CEP holder for the record. Additionally, the data presented in the Tylose C 300 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tylose C 300 DMF.
A Tylose C 300 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tylose C 300 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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