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Phyton is a World Leader in Plant Cell Fermentation Technology and Commercial Manufacturing. 
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01 Phyton Biotech LLC (1)
02 Chongqing Sintaho Pharmaceutical Co. , Ltd. (1)
03 Chongqing Taitou Pharmaceutical Co., Ltd. (2)
04 Fresenius Kabi Oncology Ltd. (1)
05 INDENA S. p. A. (1)
06 Samyang Holdings Corporation (1)
07 ScinoPharm Taiwan, Ltd. (2)
08 Sicor de Me(´)xico,S. A. de C. V. (1)
01 Docetaxel (5)
02 Docetaxel Anhydrous (1)
03 Docetaxel anhydride "Teva" (1)
04 Docetaxel anhydrous (1)
05 Docetaxel hydrate (2)
01 Canada (1)
02 Germany (1)
03 Italy (1)
04 Mexico (1)
05 South Korea (1)
06 Taiwan (2)
07 U.S.A (2)
08 Blank (1)
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PharmaCompass offers a list of Docetaxel API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Docetaxel manufacturer or Docetaxel supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Docetaxel manufacturer or Docetaxel supplier.
PharmaCompass also assists you with knowing the Docetaxel API Price utilized in the formulation of products. Docetaxel API Price is not always fixed or binding as the Docetaxel Price is obtained through a variety of data sources. The Docetaxel Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 01885_FLUKA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 01885_FLUKA, including repackagers and relabelers. The FDA regulates 01885_FLUKA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 01885_FLUKA 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 01885_FLUKA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 01885_FLUKA supplier is an individual or a company that provides 01885_FLUKA active pharmaceutical ingredient (API) or 01885_FLUKA finished formulations upon request. The 01885_FLUKA suppliers may include 01885_FLUKA API manufacturers, exporters, distributors and traders.
click here to find a list of 01885_FLUKA 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 01885_FLUKA Drug Master File in Japan (01885_FLUKA JDMF) empowers 01885_FLUKA 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 01885_FLUKA JDMF during the approval evaluation for pharmaceutical products. At the time of 01885_FLUKA 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 01885_FLUKA suppliers with JDMF on PharmaCompass.
We have 7 companies offering 01885_FLUKA
Get in contact with the supplier of your choice:
