Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.
01 1TARCHOMINSKIE ZAKLADY FARMACEUTYCZNE POLFA S.A. Warsaw PL
02 1JIANGSU HENGRUI MEDICINE CO., LTD. Lianyungang CN
01 2Ifosfamide
01 1China
02 1Poland
01 1Valid
02 1Withdrawn by Holder
Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.
Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.
Certificate Number : CEP 2006-238 - Rev 02
Status : Valid
Issue Date : 2024-08-02
Type : Chemical
Substance Number : 1529
Certificate Number : R1-CEP 2013-026 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2019-09-04
Type : Chemical
Substance Number : 1529
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PharmaCompass offers a list of Ifosfamide 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 Ifosfamide manufacturer or Ifosfamide supplier for your needs.
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PharmaCompass also assists you with knowing the Ifosfamide API Price utilized in the formulation of products. Ifosfamide API Price is not always fixed or binding as the Ifosfamide Price is obtained through a variety of data sources. The Ifosfamide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Isofosfamide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Isofosfamide, including repackagers and relabelers. The FDA regulates Isofosfamide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Isofosfamide 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 Isofosfamide supplier is an individual or a company that provides Isofosfamide active pharmaceutical ingredient (API) or Isofosfamide finished formulations upon request. The Isofosfamide suppliers may include Isofosfamide API manufacturers, exporters, distributors and traders.
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A Isofosfamide CEP of the European Pharmacopoeia monograph is often referred to as a Isofosfamide Certificate of Suitability (COS). The purpose of a Isofosfamide CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Isofosfamide EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Isofosfamide to their clients by showing that a Isofosfamide CEP has been issued for it. The manufacturer submits a Isofosfamide CEP (COS) as part of the market authorization procedure, and it takes on the role of a Isofosfamide CEP holder for the record. Additionally, the data presented in the Isofosfamide CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Isofosfamide DMF.
A Isofosfamide CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Isofosfamide 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 Isofosfamide suppliers with CEP (COS) on PharmaCompass.
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