With Fermion, start the journey of your innovative API.
01 1Fermion Oy
02 1Fuan Pharmaceutical Group Ningbo Team Pharmaceutical Co. , Ltd.
01 2Toremifene citrate
01 1China
02 1Finland
With Fermion, start the journey of your innovative API.
Registration Number : 222MF10048
Registrant's Address : Koivu-Mankkaan tie 6A, FI-02200 Espoo, Finland
Initial Date of Registration : 2010-02-09
Latest Date of Registration : 2018-08-02
Registration Number : 225MF10098
Registrant's Address : 366 Anping Road, Zhaobaoshan Street, Zhenhai District, Ningbo City, Zhejiang Province...
Initial Date of Registration : 2013-05-09
Latest Date of Registration : 2013-05-09
A Toremifene Citrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Toremifene Citrate, including repackagers and relabelers. The FDA regulates Toremifene Citrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Toremifene Citrate 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 Toremifene Citrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Toremifene Citrate supplier is an individual or a company that provides Toremifene Citrate active pharmaceutical ingredient (API) or Toremifene Citrate finished formulations upon request. The Toremifene Citrate suppliers may include Toremifene Citrate API manufacturers, exporters, distributors and traders.
click here to find a list of Toremifene Citrate 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 Toremifene Citrate Drug Master File in Japan (Toremifene Citrate JDMF) empowers Toremifene Citrate 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 Toremifene Citrate JDMF during the approval evaluation for pharmaceutical products. At the time of Toremifene Citrate 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 Toremifene Citrate suppliers with JDMF on PharmaCompass.
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