01 1NIPPON KAYAKU CO., LTD. Tokyo JP
02 1TAPI NL B.V. Amsterdam NL
03 2Zhejiang Hisun Pharmaceutical Co., Ltd. Taizhou City CN
01 3Bleomycin Sulfate
02 1Bleomycin Sulfate, Alternative process
01 2China
02 1Japan
03 1Blank
01 3Valid
02 1Withdrawn by Holder
Certificate Number : CEP 2002-149 - Rev 05
Status : Valid
Issue Date : 2023-12-12
Type : Chemical
Substance Number : 976
Bleomycin Sulfate, Alternative Process
Certificate Number : R1-CEP 2012-197 - Rev 00
Status : Valid
Issue Date : 2022-05-10
Type : Chemical
Substance Number : 976
Certificate Number : R1-CEP 2001-422 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2012-06-05
Type : Chemical
Substance Number : 976
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Certificate Number : CEP 2021-272 - Rev 02
Status : Valid
Issue Date : 2025-06-30
Type : Chemical
Substance Number : 976
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Product Web Link
Virtual Booth
Digital Content
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Corporate PDF
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PharmaCompass offers a list of Bleomycin Sulphate 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 Bleomycin Sulphate manufacturer or Bleomycin Sulphate supplier for your needs.
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A 9041-93-4 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 9041-93-4, including repackagers and relabelers. The FDA regulates 9041-93-4 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 9041-93-4 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 9041-93-4 supplier is an individual or a company that provides 9041-93-4 active pharmaceutical ingredient (API) or 9041-93-4 finished formulations upon request. The 9041-93-4 suppliers may include 9041-93-4 API manufacturers, exporters, distributors and traders.
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A 9041-93-4 CEP of the European Pharmacopoeia monograph is often referred to as a 9041-93-4 Certificate of Suitability (COS). The purpose of a 9041-93-4 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 9041-93-4 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 9041-93-4 to their clients by showing that a 9041-93-4 CEP has been issued for it. The manufacturer submits a 9041-93-4 CEP (COS) as part of the market authorization procedure, and it takes on the role of a 9041-93-4 CEP holder for the record. Additionally, the data presented in the 9041-93-4 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 9041-93-4 DMF.
A 9041-93-4 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 9041-93-4 CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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