TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
01 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
01 1Deferoxamine mesilate, Produced by fermentation
01 1Israel
01 1Valid
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Deferoxamine Mesilate, Produced By Fermentation
Certificate Number : R1-CEP 2000-160 - Rev 04
Status : Valid
Issue Date : 2022-06-17
Type : Chemical
Substance Number : 896
81
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A Desferin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Desferin, including repackagers and relabelers. The FDA regulates Desferin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Desferin 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 Desferin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Desferin supplier is an individual or a company that provides Desferin active pharmaceutical ingredient (API) or Desferin finished formulations upon request. The Desferin suppliers may include Desferin API manufacturers, exporters, distributors and traders.
click here to find a list of Desferin suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Desferin CEP of the European Pharmacopoeia monograph is often referred to as a Desferin Certificate of Suitability (COS). The purpose of a Desferin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Desferin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Desferin to their clients by showing that a Desferin CEP has been issued for it. The manufacturer submits a Desferin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Desferin CEP holder for the record. Additionally, the data presented in the Desferin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Desferin DMF.
A Desferin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Desferin 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 Desferin suppliers with CEP (COS) on PharmaCompass.
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