Phyton is a World Leader in Plant Cell Fermentation Technology and Commercial Manufacturing.
01 1Phyton Biotech LLC
02 1Chongqing Sintaho Pharmaceutical Co. , Ltd.
03 2Chongqing Taitou Pharmaceutical Co., Ltd.
04 1Fresenius Kabi Oncology Ltd.
05 1INDENA S. p. A.
06 1Samyang Holdings Corporation
07 2ScinoPharm Taiwan, Ltd.
08 1Sicor de Me(´)xico,S. A. de C. V.
Phyton is a World Leader in Plant Cell Fermentation Technology and Commercial Manufacturing.
Registration Number : 224MF10168
Registrant's Address : 1527 Cliveden Avenue, Delta, BC, Canada, V3M6P7
Initial Date of Registration : 2012-08-16
Latest Date of Registration : 2022-03-30
Chongqing Sintaho Pharma: A trusted partner globally for chemosynthetic APIs.
Registration Number : 305MF10122
Registrant's Address : No. 600, Liuqing Road, Maliuzui Town, Banan District, Chongqing, China
Initial Date of Registration : 2023-11-22
Latest Date of Registration : 2023-11-22
A Docetaxel manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Docetaxel, including repackagers and relabelers. The FDA regulates Docetaxel manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Docetaxel 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 Docetaxel manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Docetaxel supplier is an individual or a company that provides Docetaxel active pharmaceutical ingredient (API) or Docetaxel finished formulations upon request. The Docetaxel suppliers may include Docetaxel API manufacturers, exporters, distributors and traders.
click here to find a list of Docetaxel 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 Docetaxel Drug Master File in Japan (Docetaxel JDMF) empowers Docetaxel 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 Docetaxel JDMF during the approval evaluation for pharmaceutical products. At the time of Docetaxel 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 Docetaxel suppliers with JDMF on PharmaCompass.
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