Bayer AG manufactures innovative APIs and pharmaceutical formulations across diverse therapeutic areas.
01 2BAYER AG Leverkusen DE
02 1ZHEJIANG STARRY PHARMACEUTICAL CO., LTD. Xianju CN
01 2Iopromide
02 1Iopromide, 202008
01 1China
02 2Germany
01 3Valid
Bayer AG manufactures innovative APIs and pharmaceutical formulations across diverse therapeutic areas.
Bayer AG manufactures innovative APIs and pharmaceutical formulations across diverse therapeutic areas.
Certificate Number : CEP 2020-273 - Rev 01
Status : Valid
Issue Date : 2025-10-31
Type : Chemical
Substance Number : 1753
Bayer AG manufactures innovative APIs and pharmaceutical formulations across diverse therapeutic areas.
Bayer AG manufactures innovative APIs and pharmaceutical formulations across diverse therapeutic areas.
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 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, 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.
A Ultravist 300 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ultravist 300, including repackagers and relabelers. The FDA regulates Ultravist 300 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ultravist 300 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 Ultravist 300 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Ultravist 300 supplier is an individual or a company that provides Ultravist 300 active pharmaceutical ingredient (API) or Ultravist 300 finished formulations upon request. The Ultravist 300 suppliers may include Ultravist 300 API manufacturers, exporters, distributors and traders.
click here to find a list of Ultravist 300 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Ultravist 300 CEP of the European Pharmacopoeia monograph is often referred to as a Ultravist 300 Certificate of Suitability (COS). The purpose of a Ultravist 300 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Ultravist 300 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Ultravist 300 to their clients by showing that a Ultravist 300 CEP has been issued for it. The manufacturer submits a Ultravist 300 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Ultravist 300 CEP holder for the record. Additionally, the data presented in the Ultravist 300 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Ultravist 300 DMF.
A Ultravist 300 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Ultravist 300 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 Ultravist 300 suppliers with CEP (COS) on PharmaCompass.
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