01 1FORMOSA LABORATORIES, INC.
02 1GE Healthcare AS
01 2Gadodiamide hydrate
01 1Taiwan
02 1United Kingdom
Registration Number : 220MF10205
Registrant's Address : 36 Hoping Street, Louchu, Taoyuan 33842, Taiwan
Initial Date of Registration : 2008-09-29
Latest Date of Registration : 2008-11-25
Registration Number : 217MF10960
Registrant's Address : Lindesnesveien 208, 4521 Lindesnes, Norway
Initial Date of Registration : 2005-11-14
Latest Date of Registration : 2010-03-02
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PharmaCompass offers a list of Gadodiamide 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 Gadodiamide manufacturer or Gadodiamide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Gadodiamide manufacturer or Gadodiamide supplier.
PharmaCompass also assists you with knowing the Gadodiamide API Price utilized in the formulation of products. Gadodiamide API Price is not always fixed or binding as the Gadodiamide Price is obtained through a variety of data sources. The Gadodiamide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Omniscan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Omniscan, including repackagers and relabelers. The FDA regulates Omniscan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Omniscan 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 Omniscan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Omniscan supplier is an individual or a company that provides Omniscan active pharmaceutical ingredient (API) or Omniscan finished formulations upon request. The Omniscan suppliers may include Omniscan API manufacturers, exporters, distributors and traders.
click here to find a list of Omniscan 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 Omniscan Drug Master File in Japan (Omniscan JDMF) empowers Omniscan 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 Omniscan JDMF during the approval evaluation for pharmaceutical products. At the time of Omniscan 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 Omniscan suppliers with JDMF on PharmaCompass.
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