01 1GE Healthcare AS
01 1Visipaque
01 1United Kingdom
Registration Number : 217MF10958
Registrant's Address : Lindesnesveien 208, 4521 Lindesnes, Norway
Initial Date of Registration : 2005-11-14
Latest Date of Registration : 2023-11-08
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PharmaCompass offers a list of Iodixanol 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 Iodixanol manufacturer or Iodixanol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Iodixanol manufacturer or Iodixanol supplier.
PharmaCompass also assists you with knowing the Iodixanol API Price utilized in the formulation of products. Iodixanol API Price is not always fixed or binding as the Iodixanol Price is obtained through a variety of data sources. The Iodixanol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Visipaque 270 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Visipaque 270, including repackagers and relabelers. The FDA regulates Visipaque 270 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Visipaque 270 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 Visipaque 270 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Visipaque 270 supplier is an individual or a company that provides Visipaque 270 active pharmaceutical ingredient (API) or Visipaque 270 finished formulations upon request. The Visipaque 270 suppliers may include Visipaque 270 API manufacturers, exporters, distributors and traders.
click here to find a list of Visipaque 270 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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 Visipaque 270 Drug Master File in Japan (Visipaque 270 JDMF) empowers Visipaque 270 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 Visipaque 270 JDMF during the approval evaluation for pharmaceutical products. At the time of Visipaque 270 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Visipaque 270 suppliers with JDMF on PharmaCompass.
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