01 2BAYER AG Leverkusen DE
02 1ZHEJIANG STARRY PHARMACEUTICAL CO., LTD. Xianju CN
01 2Iopromide
02 1Iopromide, 202008
01 1China
02 2Germany
01 3Valid
Certificate Number : R1-CEP 2015-172 - Rev 00
Status : Valid
Issue Date : 2022-01-31
Type : Chemical
Substance Number : 1753
Certificate Number : R0-CEP 2020-273 - Rev 00
Status : Valid
Issue Date : 2021-01-06
Type : Chemical
Substance Number : 1753
Certificate Number : CEP 2022-232 - Rev 01
Status : Valid
Issue Date : 2025-05-02
Type : Chemical
Substance Number : 1753
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PharmaCompass offers a list of Iopromide 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 Iopromide manufacturer or Iopromide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Iopromide manufacturer or Iopromide supplier.
PharmaCompass also assists you with knowing the Iopromide API Price utilized in the formulation of products. Iopromide API Price is not always fixed or binding as the Iopromide Price is obtained through a variety of data sources. The Iopromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A iopromid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of iopromid, including repackagers and relabelers. The FDA regulates iopromid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. iopromid 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 iopromid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A iopromid supplier is an individual or a company that provides iopromid active pharmaceutical ingredient (API) or iopromid finished formulations upon request. The iopromid suppliers may include iopromid API manufacturers, exporters, distributors and traders.
click here to find a list of iopromid suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A iopromid CEP of the European Pharmacopoeia monograph is often referred to as a iopromid Certificate of Suitability (COS). The purpose of a iopromid CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of iopromid EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of iopromid to their clients by showing that a iopromid CEP has been issued for it. The manufacturer submits a iopromid CEP (COS) as part of the market authorization procedure, and it takes on the role of a iopromid CEP holder for the record. Additionally, the data presented in the iopromid CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the iopromid DMF.
A iopromid CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. iopromid 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 iopromid suppliers with CEP (COS) on PharmaCompass.
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