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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 SANOFI CHIMIE (1)
03 Borak Co., Ltd. (1)
04 Fresenius Kabi Oncology Limited (1)
05 Intas Pharmaceuticals Limited (1)
06 Mac-Chem Products (India) Pvt.Ltd. (1)
07 Qilu Pharmaceutical Co. Ltd (2)
08 Qilu Pharmaceutical Co., Ltd. (2)
09 Samyang Holdings Co., Ltd. (1)
10 Scinopharm Taiwan, Ltd. (2)
01 Aging Life Science Co., Ltd. (1)
02 Borak Co., Ltd. (1)
03 Eltech Pharmachem Co., Ltd. (1)
04 Gangil Chemi Farm Co., Ltd. (1)
05 Hiple Co., Ltd. (1)
06 Masung LS Co., Ltd. (1)
07 Myungmoon Pharmaceutical Co., Ltd. (2)
08 Otran Farm Korea Co., Ltd. (1)
09 Sampoong Pharmachem Co., Ltd. (1)
10 Samyang Holdings Co., Ltd. (2)
11 Sanofi-Aventis Korea Co., Ltd. (1)
01 Docetaxel Anhydrous (3)
02 Docetaxel Trihydrate (3)
03 Docetaxel hydrate (2)
04 docetaxel (5)
01 Canada (1)
02 China (4)
03 France (1)
04 India (2)
05 South Korea (1)
06 Sweden (1)
07 Taiwan (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.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a 01885_FLUKA Drug Master File in Korea (01885_FLUKA KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 01885_FLUKA. The MFDS reviews the 01885_FLUKA KDMF as part of the drug registration process and uses the information provided in the 01885_FLUKA KDMF to evaluate the safety and efficacy of the drug.
After submitting a 01885_FLUKA KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their 01885_FLUKA API can apply through the Korea Drug Master File (KDMF).
click here to find a list of 01885_FLUKA suppliers with KDMF on PharmaCompass.
We have 8 companies offering 01885_FLUKA
Get in contact with the supplier of your choice:
