01 2Dr. Paul Lohmann GmbH & Co. KGaA
01 2Drying of iron sulfate
01 2Germany
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
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
A Ferrous Sulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ferrous Sulfate, including repackagers and relabelers. The FDA regulates Ferrous Sulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ferrous Sulfate 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 Ferrous Sulfate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ferrous Sulfate supplier is an individual or a company that provides Ferrous Sulfate active pharmaceutical ingredient (API) or Ferrous Sulfate finished formulations upon request. The Ferrous Sulfate suppliers may include Ferrous Sulfate API manufacturers, exporters, distributors and traders.
click here to find a list of Ferrous Sulfate 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 Ferrous Sulfate Drug Master File in Japan (Ferrous Sulfate JDMF) empowers Ferrous Sulfate 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 Ferrous Sulfate JDMF during the approval evaluation for pharmaceutical products. At the time of Ferrous Sulfate 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 Ferrous Sulfate suppliers with JDMF on PharmaCompass.
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