Phyton is a World Leader in Plant Cell Fermentation Technology and Commercial Manufacturing.
01 1Phyton Biotech LLC
02 1TAPI Czech Industries s. r. o.
03 1Corden Pharma Boulder, Inc.
04 3INDENA S. p. A.
05 1Samyang Holdings Corporation
06 1ScinoPharm Taiwan, Ltd.
07 1Yunnan Hande Bio-Tech Co. , Ltd.
08 1Zhejiang Starry Pharmaceutical Co. ,Ltd
Phyton is a World Leader in Plant Cell Fermentation Technology and Commercial Manufacturing.
Registration Number : 224MF10111
Registrant's Address : 1527 Cliveden Avenue, Delta, BC, Canada, V3M6P7
Initial Date of Registration : 2012-07-04
Latest Date of Registration : 2020-06-19
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Registration Number : 305MF10109
Registrant's Address : Ostravska 305/29, Komarov, 747 70 Opava, Czech Republic
Initial Date of Registration : 2023-09-20
Latest Date of Registration : 2023-09-20
A Paclitaxel manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Paclitaxel, including repackagers and relabelers. The FDA regulates Paclitaxel manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Paclitaxel 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 Paclitaxel manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Paclitaxel supplier is an individual or a company that provides Paclitaxel active pharmaceutical ingredient (API) or Paclitaxel finished formulations upon request. The Paclitaxel suppliers may include Paclitaxel API manufacturers, exporters, distributors and traders.
click here to find a list of Paclitaxel 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 Paclitaxel Drug Master File in Japan (Paclitaxel JDMF) empowers Paclitaxel 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 Paclitaxel JDMF during the approval evaluation for pharmaceutical products. At the time of Paclitaxel 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 Paclitaxel suppliers with JDMF on PharmaCompass.
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