01 1Dr. Paul Lohmann GmbH & Co. KGaA
01 1Ferrous fumarate
01 1Germany
Registration Number : 221MF10120
Registrant's Address : Hauptstrasse 2 D-31860 Emmerthal Germany
Initial Date of Registration : 2009-06-16
Latest Date of Registration : 2009-06-16
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PharmaCompass offers a list of Ferrous Fumarate 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 Fumarate manufacturer or Ferrous Fumarate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ferrous Fumarate manufacturer or Ferrous Fumarate supplier.
PharmaCompass also assists you with knowing the Ferrous Fumarate API Price utilized in the formulation of products. Ferrous Fumarate API Price is not always fixed or binding as the Ferrous Fumarate Price is obtained through a variety of data sources. The Ferrous Fumarate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ferrotemp manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ferrotemp, including repackagers and relabelers. The FDA regulates Ferrotemp manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ferrotemp 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 Ferrotemp manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ferrotemp supplier is an individual or a company that provides Ferrotemp active pharmaceutical ingredient (API) or Ferrotemp finished formulations upon request. The Ferrotemp suppliers may include Ferrotemp API manufacturers, exporters, distributors and traders.
click here to find a list of Ferrotemp suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Ferrotemp Drug Master File in Japan (Ferrotemp JDMF) empowers Ferrotemp API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Ferrotemp JDMF during the approval evaluation for pharmaceutical products. At the time of Ferrotemp JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Ferrotemp suppliers with JDMF on PharmaCompass.
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