Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
01 1PCAS S.A.
02 2Excella GmbH & Co. K.G.
03 1Yangtze River Pharmaceutical Group Jiangsu Haici Biological Pharmaceutical Co. ,Ltd
01 2Tamoxifen Citrate
02 2Tamoxifen citrate
01 1France
02 1Germany
03 1Luxembourg
04 1Blank
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
Registration Number : 218MF10150
Registrant's Address : 21, chemin de la Sauvegarde 21 Ecully Parc - CS 33167 69134 Ecully Cedex France
Initial Date of Registration : 2006-01-31
Latest Date of Registration : 2008-04-21
Registration Number : 306MF10097
Registrant's Address : NUERNBERGER STRASSE 12, 90537 FEUCHT, GERMANY
Initial Date of Registration : 2024-07-11
Latest Date of Registration : 2024-07-11
Registration Number : 219MF10242
Registrant's Address : NUERNBERGER STRASSE 12, 90537 FEUCHT, GERMANY
Initial Date of Registration : 2007-07-17
Latest Date of Registration : 2021-03-17
Registration Number : 306MF10120
Registrant's Address : 8 Taizhen Road, Medical New & Hi-tech Industrial Development Zone, Taizhou, Jiangsu, ...
Initial Date of Registration : 2024-09-11
Latest Date of Registration : 2024-09-11
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A Tamoxifen Citrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tamoxifen Citrate, including repackagers and relabelers. The FDA regulates Tamoxifen Citrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tamoxifen 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 Tamoxifen Citrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tamoxifen Citrate supplier is an individual or a company that provides Tamoxifen Citrate active pharmaceutical ingredient (API) or Tamoxifen Citrate finished formulations upon request. The Tamoxifen Citrate suppliers may include Tamoxifen Citrate API manufacturers, exporters, distributors and traders.
click here to find a list of Tamoxifen 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 Tamoxifen Citrate Drug Master File in Japan (Tamoxifen Citrate JDMF) empowers Tamoxifen 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 Tamoxifen Citrate JDMF during the approval evaluation for pharmaceutical products. At the time of Tamoxifen 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 Tamoxifen Citrate suppliers with JDMF on PharmaCompass.
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