01 2DR. PAUL LOHMANN GMBH & CO. KGAA Emmerthal DE
01 1Ferrous sulfate heptahydrate
02 1Ferrous sulfate, dried, Powder, milled powder, micronised powder
01 2Germany
01 2Valid
Ferrous Sulfate, Dried, Powder, Milled Powder, M...
Certificate Number : R1-CEP 2007-368 - Rev 04
Status : Valid
Issue Date : 2022-01-28
Type : Chemical
Substance Number : 2340
Certificate Number : R1-CEP 2007-369 - Rev 03
Status : Valid
Issue Date : 2022-02-01
Type : Chemical
Substance Number : 83
81
PharmaCompass offers a list of Ferrous Sulfate 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 Ferrous Sulfate manufacturer or Ferrous Sulfate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ferrous Sulfate manufacturer or Ferrous Sulfate supplier.
PharmaCompass also assists you with knowing the Ferrous Sulfate API Price utilized in the formulation of products. Ferrous Sulfate API Price is not always fixed or binding as the Ferrous Sulfate Price is obtained through a variety of data sources. The Ferrous Sulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Aktiferrin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aktiferrin, including repackagers and relabelers. The FDA regulates Aktiferrin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aktiferrin 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 Aktiferrin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aktiferrin supplier is an individual or a company that provides Aktiferrin active pharmaceutical ingredient (API) or Aktiferrin finished formulations upon request. The Aktiferrin suppliers may include Aktiferrin API manufacturers, exporters, distributors and traders.
click here to find a list of Aktiferrin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Aktiferrin CEP of the European Pharmacopoeia monograph is often referred to as a Aktiferrin Certificate of Suitability (COS). The purpose of a Aktiferrin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Aktiferrin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Aktiferrin to their clients by showing that a Aktiferrin CEP has been issued for it. The manufacturer submits a Aktiferrin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Aktiferrin CEP holder for the record. Additionally, the data presented in the Aktiferrin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Aktiferrin DMF.
A Aktiferrin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Aktiferrin 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 Aktiferrin suppliers with CEP (COS) on PharmaCompass.
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