Dr. Paul Lohmann® provides premium mineral salts backed by 140+ years of innovation, quality manufacturing, and global expertise.
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
Dr. Paul Lohmann® provides premium mineral salts backed by 140+ years of innovation, quality manufacturing, and global expertise.
Dr. Paul Lohmann® provides premium mineral salts backed by 140+ years of innovation, quality manufacturing, and global expertise.
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
Dr. Paul Lohmann® provides premium mineral salts backed by 140+ years of innovation, quality manufacturing, and global expertise.
Dr. Paul Lohmann® provides premium mineral salts backed by 140+ years of innovation, quality manufacturing, and global expertise.
Certificate Number : R1-CEP 2007-369 - Rev 03
Status : Valid
Issue Date : 2022-02-01
Type : Chemical
Substance Number : 83
18
PharmaCompass offers a list of Ferrous Sulfate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, 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.
A FT-0626420 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of FT-0626420, including repackagers and relabelers. The FDA regulates FT-0626420 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. FT-0626420 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 FT-0626420 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A FT-0626420 supplier is an individual or a company that provides FT-0626420 active pharmaceutical ingredient (API) or FT-0626420 finished formulations upon request. The FT-0626420 suppliers may include FT-0626420 API manufacturers, exporters, distributors and traders.
click here to find a list of FT-0626420 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A FT-0626420 CEP of the European Pharmacopoeia monograph is often referred to as a FT-0626420 Certificate of Suitability (COS). The purpose of a FT-0626420 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of FT-0626420 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of FT-0626420 to their clients by showing that a FT-0626420 CEP has been issued for it. The manufacturer submits a FT-0626420 CEP (COS) as part of the market authorization procedure, and it takes on the role of a FT-0626420 CEP holder for the record. Additionally, the data presented in the FT-0626420 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the FT-0626420 DMF.
A FT-0626420 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. FT-0626420 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 FT-0626420 suppliers with CEP (COS) on PharmaCompass.
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