With Fermion, start the journey of your innovative API.
01 1Fermion Oy
02 1Excella GmbH & Co. K.G.
03 2HUZHOU ZHANWANG PHARMACEUTICAL CO. ,LTD
01 4Methotrexate
01 2China
02 1Finland
03 1Luxembourg
With Fermion, start the journey of your innovative API.
Registration Number : 219MF10359
Registrant's Address : Koivu-Mankkaan tie 6A, FI-02200 Espoo, Finland
Initial Date of Registration : 2007-12-13
Latest Date of Registration : 2018-05-15
Registration Number : 219MF10360
Registrant's Address : NUERNBERGER STRASSE 12, 90537 FEUCHT, GERMANY
Initial Date of Registration : 2007-12-13
Latest Date of Registration : 2024-11-27
Registration Number : 229MF10125
Registrant's Address : West Development Area, Linghu Town, Huzhou City, 313018, Zhejiang Province, China
Initial Date of Registration : 2017-07-14
Latest Date of Registration : 2017-07-14
Registration Number : 220MF10179
Registrant's Address : West Development Area, Linghu Town, Huzhou City, 313018, Zhejiang Province, China
Initial Date of Registration : 2008-07-31
Latest Date of Registration : 2018-03-14
A Methotrexate Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methotrexate Sodium, including repackagers and relabelers. The FDA regulates Methotrexate Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methotrexate Sodium 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 Methotrexate Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Methotrexate Sodium supplier is an individual or a company that provides Methotrexate Sodium active pharmaceutical ingredient (API) or Methotrexate Sodium finished formulations upon request. The Methotrexate Sodium suppliers may include Methotrexate Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Methotrexate Sodium 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 Methotrexate Sodium Drug Master File in Japan (Methotrexate Sodium JDMF) empowers Methotrexate Sodium 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 Methotrexate Sodium JDMF during the approval evaluation for pharmaceutical products. At the time of Methotrexate Sodium 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 Methotrexate Sodium suppliers with JDMF on PharmaCompass.
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