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
60
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 Cellogen WS-C manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cellogen WS-C, including repackagers and relabelers. The FDA regulates Cellogen WS-C manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cellogen WS-C 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 Cellogen WS-C supplier is an individual or a company that provides Cellogen WS-C active pharmaceutical ingredient (API) or Cellogen WS-C finished formulations upon request. The Cellogen WS-C suppliers may include Cellogen WS-C API manufacturers, exporters, distributors and traders.
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A Cellogen WS-C CEP of the European Pharmacopoeia monograph is often referred to as a Cellogen WS-C Certificate of Suitability (COS). The purpose of a Cellogen WS-C CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cellogen WS-C EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cellogen WS-C to their clients by showing that a Cellogen WS-C CEP has been issued for it. The manufacturer submits a Cellogen WS-C CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cellogen WS-C CEP holder for the record. Additionally, the data presented in the Cellogen WS-C CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cellogen WS-C DMF.
A Cellogen WS-C CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cellogen WS-C 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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