Phyton is a World Leader in Plant Cell Fermentation Technology and Commercial Manufacturing.
01 1PHYTON BIOTECH LLC Delta CA
02 1SANOFI WINTHROP INDUSTRIE Gentilly FR
03 1CHONGQING SINTAHO PHARMACEUTICAL CO., LTD. Maliuzui CN
04 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
05 2FRESENIUS KABI ONCOLOGY LIMITED Kalyani IN
06 2Fujian South Pharmaceutical Co., Ltd. Sanming City CN
07 1HETERO LABS LIMITED Hyderabad IN
08 2HUBEI HAOSUN PHARMACEUTICAL CO., LTD. Ezhou CN
09 2INDENA S.P.A. Milano IT
10 2INTAS PHARMACEUTICALS LIMITED Ahmedabad IN
11 1INTAS PHARMACEUTICALS LIMITED North Harrow GB
12 1LAURUS LABS LIMITED Hyderabad IN
13 2MSN LABORATORIES PRIVATE LIMITED Kardanur Village IN
14 2POLYMED THERAPEUTICS, INC. Houston US
15 2QILU PHARMACEUTICAL CO., LTD. Jinan CN
16 1SAMYANG BIOPHARMACEUTICALS CORPORATION Daejeon KR
17 1SAMYANG HOLDINGS CORPORATION Gyeonggi-do KR
18 2SCINOPHARM TAIWAN, LTD. Shan-Hua TW
19 1WUHAN CALMLAND PHARMACEUTICALS CO., LTD. Wuhan CN
20 1Zhejiang Hisun Pharmaceutical Co., Ltd. Taizhou City CN
Phyton is a World Leader in Plant Cell Fermentation Technology and Commercial Manufacturing.
Certificate Number : R1-CEP 2012-105 - Rev 01
Status : Valid
Issue Date : 2019-10-08
Type : Chemical
Substance Number : 2593
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Certificate Number : CEP 2009-343 - Rev 04
Status : Valid
Issue Date : 2024-03-28
Type : Chemical
Substance Number : 2449
Chongqing Sintaho Pharma: A trusted partner globally for chemosynthetic APIs.
Certificate Number : CEP 2022-295 - Rev 00
Status : Valid
Issue Date : 2023-09-28
Type : Chemical
Substance Number : 2593
A Docetaxel Anhydrous manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Docetaxel Anhydrous, including repackagers and relabelers. The FDA regulates Docetaxel Anhydrous manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Docetaxel Anhydrous API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Docetaxel Anhydrous supplier is an individual or a company that provides Docetaxel Anhydrous active pharmaceutical ingredient (API) or Docetaxel Anhydrous finished formulations upon request. The Docetaxel Anhydrous suppliers may include Docetaxel Anhydrous API manufacturers, exporters, distributors and traders.
click here to find a list of Docetaxel Anhydrous suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Docetaxel Anhydrous CEP of the European Pharmacopoeia monograph is often referred to as a Docetaxel Anhydrous Certificate of Suitability (COS). The purpose of a Docetaxel Anhydrous CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Docetaxel Anhydrous EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Docetaxel Anhydrous to their clients by showing that a Docetaxel Anhydrous CEP has been issued for it. The manufacturer submits a Docetaxel Anhydrous CEP (COS) as part of the market authorization procedure, and it takes on the role of a Docetaxel Anhydrous CEP holder for the record. Additionally, the data presented in the Docetaxel Anhydrous CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Docetaxel Anhydrous DMF.
A Docetaxel Anhydrous CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Docetaxel Anhydrous CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Docetaxel Anhydrous suppliers with CEP (COS) on PharmaCompass.
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