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01 2Mingtai Chemical Co., Ltd. Taoyuan Hsien TW
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01 1Croscarmellose sodium
02 1Croscarmellose sodium, Process II
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01 2China
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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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PharmaCompass also assists you with knowing the Sodium Carboxymethylcellulose API Price utilized in the formulation of products. Sodium Carboxymethylcellulose API Price is not always fixed or binding as the Sodium Carboxymethylcellulose Price is obtained through a variety of data sources. The Sodium Carboxymethylcellulose Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CMC 7M manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CMC 7M, including repackagers and relabelers. The FDA regulates CMC 7M manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CMC 7M 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 CMC 7M supplier is an individual or a company that provides CMC 7M active pharmaceutical ingredient (API) or CMC 7M finished formulations upon request. The CMC 7M suppliers may include CMC 7M API manufacturers, exporters, distributors and traders.
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A CMC 7M CEP of the European Pharmacopoeia monograph is often referred to as a CMC 7M Certificate of Suitability (COS). The purpose of a CMC 7M CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of CMC 7M EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of CMC 7M to their clients by showing that a CMC 7M CEP has been issued for it. The manufacturer submits a CMC 7M CEP (COS) as part of the market authorization procedure, and it takes on the role of a CMC 7M CEP holder for the record. Additionally, the data presented in the CMC 7M CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the CMC 7M DMF.
A CMC 7M CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. CMC 7M 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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