Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
01 1TRANSO-PHARM HANDELS GMBH Siek DE
02 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
03 1Adorkem Technology S.p.A. Costa Volpino IT
04 2BORYUNG PHARMACEUTICAL CO., LTD. Seoul KR
05 1DZD (HEZE) PHARMACEUTICAL CO., LTD. Heze City CN
06 1INTAS PHARMACEUTICALS LIMITED Ahmedabad IN
07 1MEIJI SEIKA PHARMA CO., LTD. Tokyo JP
08 1MICROBIOPHARM JAPAN CO., LTD. Tokyo JP
09 1OLON S.P.A. Rodano IT
10 1STERLING BIOTECH LIMITED Masar Village IN
11 1SYNBIAS PHARMA AG Schaffhausen CH
12 2Zhejiang Hisun Pharmaceutical Co., Ltd. Taizhou City CN
Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
Certificate Number : R1-CEP 2004-059 - Rev 03
Status : Valid
Issue Date : 2023-03-06
Type : Chemical
Substance Number : 714
TAPI offers customized CDMO Solutions for API development and manufacturing services.
Certificate Number : CEP 2003-111 - Rev 06
Status : Valid
Issue Date : 2024-05-29
Type : Chemical
Substance Number : 714
A Doxorubicin Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Doxorubicin Hydrochloride, including repackagers and relabelers. The FDA regulates Doxorubicin Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Doxorubicin Hydrochloride 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 Doxorubicin Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Doxorubicin Hydrochloride supplier is an individual or a company that provides Doxorubicin Hydrochloride active pharmaceutical ingredient (API) or Doxorubicin Hydrochloride finished formulations upon request. The Doxorubicin Hydrochloride suppliers may include Doxorubicin Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Doxorubicin Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Doxorubicin Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Doxorubicin Hydrochloride Certificate of Suitability (COS). The purpose of a Doxorubicin Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Doxorubicin Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Doxorubicin Hydrochloride to their clients by showing that a Doxorubicin Hydrochloride CEP has been issued for it. The manufacturer submits a Doxorubicin Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Doxorubicin Hydrochloride CEP holder for the record. Additionally, the data presented in the Doxorubicin Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Doxorubicin Hydrochloride DMF.
A Doxorubicin Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Doxorubicin Hydrochloride 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 Doxorubicin Hydrochloride suppliers with CEP (COS) on PharmaCompass.
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