01 1BRACCO IMAGING S. P. A.
02 1DongKook Life Science Co. , Ltd.
03 3Zhejiang Starry Pharmaceutical Co. ,Ltd
04 1Zhejiang Taizhou Hisyn Pharmaceutical Co. , Ltd.
01 1Iopamidel
02 5Iopamidol
01 4China
02 1Italy
03 1South Korea
Registration Number : 302MF10145
Registrant's Address : Via Egidio Folli, 50-20134 Milano (MI), ITALY
Initial Date of Registration : 2020-12-15
Latest Date of Registration : 2025-02-13
Registration Number : 217MF10576
Registrant's Address : 7, Teheran-ro 108-gil, Gangnam-gu, Seoul, Korea
Initial Date of Registration : 2005-09-14
Latest Date of Registration : 2019-01-10
Registration Number : 225MF10207
Registrant's Address : No. 1 Starry Road of Xianju Modern Industrial Centralization Zone, Xianju, Zhejiang, ...
Initial Date of Registration : 2013-11-14
Latest Date of Registration : 2013-11-14
Registration Number : 304MF10133
Registrant's Address : No. 1 Starry Road of Xianju Modern Industrial Centralization Zone, Xianju, Zhejiang, ...
Initial Date of Registration : 2022-09-21
Latest Date of Registration : 2022-09-21
Registration Number : 304MF10132
Registrant's Address : No. 1 Starry Road of Xianju Modern Industrial Centralization Zone, Xianju, Zhejiang, ...
Initial Date of Registration : 2022-09-21
Latest Date of Registration : 2022-09-21
Registration Number : 227MF10103
Registrant's Address : Zhejiang Province Chemical and Medical Materials Base, Linhai Park
Initial Date of Registration : 2015-04-09
Latest Date of Registration : 2015-04-09
15
PharmaCompass offers a list of Iopamidol 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 Iopamidol manufacturer or Iopamidol supplier for your needs.
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A Isovue 370 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Isovue 370, including repackagers and relabelers. The FDA regulates Isovue 370 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Isovue 370 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 Isovue 370 supplier is an individual or a company that provides Isovue 370 active pharmaceutical ingredient (API) or Isovue 370 finished formulations upon request. The Isovue 370 suppliers may include Isovue 370 API manufacturers, exporters, distributors and traders.
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The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Isovue 370 Drug Master File in Japan (Isovue 370 JDMF) empowers Isovue 370 API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Isovue 370 JDMF during the approval evaluation for pharmaceutical products. At the time of Isovue 370 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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