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
02 1EXCELLA GMBH & CO. KG Feucht DE
01 1Deferoxamine mesilate, Produced by a synthetic process
02 1Deferoxamine mesilate, Produced by fermentation
01 1Gabon
02 1Israel
01 2Valid
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
Deferoxamine Mesilate, Produced By A Synthetic P...
Certificate Number : CEP 2009-401 - Rev 06
Status : Valid
Issue Date : 2025-03-11
Type : Chemical
Substance Number : 896
17
PharmaCompass offers a list of Deferoxamine Mesylate 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 Deferoxamine Mesylate manufacturer or Deferoxamine Mesylate supplier for your needs.
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PharmaCompass also assists you with knowing the Deferoxamine Mesylate API Price utilized in the formulation of products. Deferoxamine Mesylate API Price is not always fixed or binding as the Deferoxamine Mesylate Price is obtained through a variety of data sources. The Deferoxamine Mesylate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A D9533_SIGMA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of D9533_SIGMA, including repackagers and relabelers. The FDA regulates D9533_SIGMA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. D9533_SIGMA 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 D9533_SIGMA supplier is an individual or a company that provides D9533_SIGMA active pharmaceutical ingredient (API) or D9533_SIGMA finished formulations upon request. The D9533_SIGMA suppliers may include D9533_SIGMA API manufacturers, exporters, distributors and traders.
click here to find a list of D9533_SIGMA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A D9533_SIGMA CEP of the European Pharmacopoeia monograph is often referred to as a D9533_SIGMA Certificate of Suitability (COS). The purpose of a D9533_SIGMA CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of D9533_SIGMA EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of D9533_SIGMA to their clients by showing that a D9533_SIGMA CEP has been issued for it. The manufacturer submits a D9533_SIGMA CEP (COS) as part of the market authorization procedure, and it takes on the role of a D9533_SIGMA CEP holder for the record. Additionally, the data presented in the D9533_SIGMA CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the D9533_SIGMA DMF.
A D9533_SIGMA CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. D9533_SIGMA 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 D9533_SIGMA suppliers with CEP (COS) on PharmaCompass.
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