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