01 2Dr. Paul Lohmann GmbH & Co. KGaA
01 2Drying of iron sulfate
01 2Germany
Registration Number : 218MF10655
Registrant's Address : Hauptstrasse 2 D-31860 Emmerthal Germany
Initial Date of Registration : 2006-07-24
Latest Date of Registration : 2006-07-24
Registration Number : 221MF10113
Registrant's Address : Hauptstrasse 2 D-31860 Emmerthal Germany
Initial Date of Registration : 2009-06-10
Latest Date of Registration : 2009-06-10
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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 biofer manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of biofer, including repackagers and relabelers. The FDA regulates biofer manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. biofer 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 biofer manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A biofer supplier is an individual or a company that provides biofer active pharmaceutical ingredient (API) or biofer finished formulations upon request. The biofer suppliers may include biofer API manufacturers, exporters, distributors and traders.
click here to find a list of biofer 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 biofer Drug Master File in Japan (biofer JDMF) empowers biofer 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 biofer JDMF during the approval evaluation for pharmaceutical products. At the time of biofer 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 biofer suppliers with JDMF on PharmaCompass.
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