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 Galfer manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Galfer, including repackagers and relabelers. The FDA regulates Galfer manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Galfer 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 Galfer manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Galfer supplier is an individual or a company that provides Galfer active pharmaceutical ingredient (API) or Galfer finished formulations upon request. The Galfer suppliers may include Galfer API manufacturers, exporters, distributors and traders.
click here to find a list of Galfer 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 Galfer Drug Master File in Japan (Galfer JDMF) empowers Galfer 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 Galfer JDMF during the approval evaluation for pharmaceutical products. At the time of Galfer JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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