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 : R0-CEP 2020-273 - Rev 00
Status : Valid
Issue Date : 2021-01-06
Type : Chemical
Substance Number : 1753
Certificate Number : R1-CEP 2015-172 - Rev 00
Status : Valid
Issue Date : 2022-01-31
Type : Chemical
Substance Number : 1753
Certificate Number : CEP 2022-232 - Rev 00
Status : Valid
Issue Date : 2024-07-16
Type : Chemical
Substance Number : 1753
A Iopromide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Iopromide, including repackagers and relabelers. The FDA regulates Iopromide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Iopromide 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 Iopromide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Iopromide supplier is an individual or a company that provides Iopromide active pharmaceutical ingredient (API) or Iopromide finished formulations upon request. The Iopromide suppliers may include Iopromide API manufacturers, exporters, distributors and traders.
click here to find a list of Iopromide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Iopromide CEP of the European Pharmacopoeia monograph is often referred to as a Iopromide Certificate of Suitability (COS). The purpose of a Iopromide CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Iopromide EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Iopromide to their clients by showing that a Iopromide CEP has been issued for it. The manufacturer submits a Iopromide CEP (COS) as part of the market authorization procedure, and it takes on the role of a Iopromide CEP holder for the record. Additionally, the data presented in the Iopromide CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Iopromide DMF.
A Iopromide CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Iopromide 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 Iopromide suppliers with CEP (COS) on PharmaCompass.
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