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 00
Status : Valid
Issue Date : 2024-07-16
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.
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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 ULTRAVIST 300 IN PLASTIC CONTAINER manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ULTRAVIST 300 IN PLASTIC CONTAINER, including repackagers and relabelers. The FDA regulates ULTRAVIST 300 IN PLASTIC CONTAINER manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ULTRAVIST 300 IN PLASTIC CONTAINER 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 ULTRAVIST 300 IN PLASTIC CONTAINER supplier is an individual or a company that provides ULTRAVIST 300 IN PLASTIC CONTAINER active pharmaceutical ingredient (API) or ULTRAVIST 300 IN PLASTIC CONTAINER finished formulations upon request. The ULTRAVIST 300 IN PLASTIC CONTAINER suppliers may include ULTRAVIST 300 IN PLASTIC CONTAINER API manufacturers, exporters, distributors and traders.
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A ULTRAVIST 300 IN PLASTIC CONTAINER CEP of the European Pharmacopoeia monograph is often referred to as a ULTRAVIST 300 IN PLASTIC CONTAINER Certificate of Suitability (COS). The purpose of a ULTRAVIST 300 IN PLASTIC CONTAINER CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of ULTRAVIST 300 IN PLASTIC CONTAINER EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of ULTRAVIST 300 IN PLASTIC CONTAINER to their clients by showing that a ULTRAVIST 300 IN PLASTIC CONTAINER CEP has been issued for it. The manufacturer submits a ULTRAVIST 300 IN PLASTIC CONTAINER CEP (COS) as part of the market authorization procedure, and it takes on the role of a ULTRAVIST 300 IN PLASTIC CONTAINER CEP holder for the record. Additionally, the data presented in the ULTRAVIST 300 IN PLASTIC CONTAINER CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the ULTRAVIST 300 IN PLASTIC CONTAINER DMF.
A ULTRAVIST 300 IN PLASTIC CONTAINER CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. ULTRAVIST 300 IN PLASTIC CONTAINER 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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