01 1CHROMO LABORATORIES INDIA PRIVATE LIMITED Pashamylaram IN
02 1MSN LIFE SCIENCES PRIVATE LIMITED Chandampet Village IN
01 1Ziprasidone mesilate trihydrate
02 1Ziprasidone mesilate trihydrate, Crystalline Form
01 2India
01 2Valid
Ziprasidone Mesilate Trihydrate
Certificate Number : CEP 2022-452 - Rev 00
Status : Valid
Issue Date : 2024-08-16
Type : Chemical
Substance Number : 2649
Ziprasidone Mesilate Trihydrate, Crystalline For...
Certificate Number : CEP 2021-440 - Rev 00
Status : Valid
Issue Date : 2024-03-13
Type : Chemical
Substance Number : 2649
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PharmaCompass offers a list of CHEBI:53757 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 CHEBI:53757 manufacturer or CHEBI:53757 supplier for your needs.
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A CHEBI:53757 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CHEBI:53757, including repackagers and relabelers. The FDA regulates CHEBI:53757 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CHEBI:53757 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A CHEBI:53757 supplier is an individual or a company that provides CHEBI:53757 active pharmaceutical ingredient (API) or CHEBI:53757 finished formulations upon request. The CHEBI:53757 suppliers may include CHEBI:53757 API manufacturers, exporters, distributors and traders.
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A CHEBI:53757 CEP of the European Pharmacopoeia monograph is often referred to as a CHEBI:53757 Certificate of Suitability (COS). The purpose of a CHEBI:53757 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of CHEBI:53757 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of CHEBI:53757 to their clients by showing that a CHEBI:53757 CEP has been issued for it. The manufacturer submits a CHEBI:53757 CEP (COS) as part of the market authorization procedure, and it takes on the role of a CHEBI:53757 CEP holder for the record. Additionally, the data presented in the CHEBI:53757 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the CHEBI:53757 DMF.
A CHEBI:53757 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. CHEBI:53757 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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