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
A Croscarmellose Sodium API manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Croscarmellose Sodium API, including repackagers and relabelers. The FDA regulates Croscarmellose Sodium API manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Croscarmellose Sodium API API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Croscarmellose Sodium API manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Croscarmellose Sodium API supplier is an individual or a company that provides Croscarmellose Sodium API active pharmaceutical ingredient (API) or Croscarmellose Sodium API finished formulations upon request. The Croscarmellose Sodium API suppliers may include Croscarmellose Sodium API API manufacturers, exporters, distributors and traders.
click here to find a list of Croscarmellose Sodium API suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Croscarmellose Sodium API CEP of the European Pharmacopoeia monograph is often referred to as a Croscarmellose Sodium API Certificate of Suitability (COS). The purpose of a Croscarmellose Sodium API CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Croscarmellose Sodium API EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Croscarmellose Sodium API to their clients by showing that a Croscarmellose Sodium API CEP has been issued for it. The manufacturer submits a Croscarmellose Sodium API CEP (COS) as part of the market authorization procedure, and it takes on the role of a Croscarmellose Sodium API CEP holder for the record. Additionally, the data presented in the Croscarmellose Sodium API CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Croscarmellose Sodium API DMF.
A Croscarmellose Sodium API CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Croscarmellose Sodium API CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Croscarmellose Sodium API suppliers with CEP (COS) on PharmaCompass.
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