01 1DR. PAUL LOHMANN GMBH & CO. KGAA Emmerthal DE
02 1FERROPHARMA CHEMICALS LTD. Dóc HU
03 1POLYDRUG LABORATORIES PVT. LTD. Mumbai IN
01 3Ferrous fumarate
01 1Germany
02 1India
03 1Indonesia
01 2Valid
02 1Withdrawn by EDQM Failure to CEP procedure
Certificate Number : R1-CEP 2004-232 - Rev 03
Status : Valid
Issue Date : 2021-07-13
Type : Chemical
Substance Number : 902
Certificate Number : R1-CEP 2012-400 - Rev 00
Status : Valid
Issue Date : 2020-02-19
Type : Chemical
Substance Number : 902
Certificate Number : R0-CEP 2010-147 - Rev 00
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2012-02-22
Type : Chemical
Substance Number : 902
A Ferrous Fumarate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ferrous Fumarate, including repackagers and relabelers. The FDA regulates Ferrous Fumarate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ferrous Fumarate 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 Ferrous Fumarate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ferrous Fumarate supplier is an individual or a company that provides Ferrous Fumarate active pharmaceutical ingredient (API) or Ferrous Fumarate finished formulations upon request. The Ferrous Fumarate suppliers may include Ferrous Fumarate API manufacturers, exporters, distributors and traders.
click here to find a list of Ferrous Fumarate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ferrous Fumarate CEP of the European Pharmacopoeia monograph is often referred to as a Ferrous Fumarate Certificate of Suitability (COS). The purpose of a Ferrous Fumarate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Ferrous Fumarate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Ferrous Fumarate to their clients by showing that a Ferrous Fumarate CEP has been issued for it. The manufacturer submits a Ferrous Fumarate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Ferrous Fumarate CEP holder for the record. Additionally, the data presented in the Ferrous Fumarate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Ferrous Fumarate DMF.
A Ferrous Fumarate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Ferrous Fumarate 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 Ferrous Fumarate suppliers with CEP (COS) on PharmaCompass.
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