01 1Guerbet Ireland ULC
01 1Ioversol
01 1Ireland
Registration Number : 226MF10059
Registrant's Address : Damastown, Mulhuddart, Dublin 15 Ireland
Initial Date of Registration : 2014-03-06
Latest Date of Registration : 2014-03-06
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PharmaCompass offers a list of Ioversol 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 Ioversol manufacturer or Ioversol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ioversol manufacturer or Ioversol supplier.
PharmaCompass also assists you with knowing the Ioversol API Price utilized in the formulation of products. Ioversol API Price is not always fixed or binding as the Ioversol Price is obtained through a variety of data sources. The Ioversol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Optiray 350 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Optiray 350, including repackagers and relabelers. The FDA regulates Optiray 350 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Optiray 350 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 Optiray 350 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Optiray 350 supplier is an individual or a company that provides Optiray 350 active pharmaceutical ingredient (API) or Optiray 350 finished formulations upon request. The Optiray 350 suppliers may include Optiray 350 API manufacturers, exporters, distributors and traders.
click here to find a list of Optiray 350 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 Optiray 350 Drug Master File in Japan (Optiray 350 JDMF) empowers Optiray 350 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 Optiray 350 JDMF during the approval evaluation for pharmaceutical products. At the time of Optiray 350 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 Optiray 350 suppliers with JDMF on PharmaCompass.
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