01 1Ace Japan Co., Ltd.
02 1Yakumo Chemical Industry Co., Ltd.
01 1Bromide tiquizium
02 1Tiquizium bromide
01 1Japan
02 1Blank
Registration Number : 220MF10237
Registrant's Address : Yamagata Prefecture Higashine City Higashine City 5850-1
Initial Date of Registration : 2008-11-25
Latest Date of Registration : 2008-11-25
Registration Number : 221MF10145
Registrant's Address : Osaka Prefecture Higashiosaka City Kamiishikiricho 2-1378
Initial Date of Registration : 2009-07-09
Latest Date of Registration : 2009-07-09
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A Tiquizium Bromide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tiquizium Bromide, including repackagers and relabelers. The FDA regulates Tiquizium Bromide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tiquizium Bromide API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Tiquizium Bromide supplier is an individual or a company that provides Tiquizium Bromide active pharmaceutical ingredient (API) or Tiquizium Bromide finished formulations upon request. The Tiquizium Bromide suppliers may include Tiquizium Bromide API manufacturers, exporters, distributors and traders.
click here to find a list of Tiquizium Bromide 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 Tiquizium Bromide Drug Master File in Japan (Tiquizium Bromide JDMF) empowers Tiquizium Bromide 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 Tiquizium Bromide JDMF during the approval evaluation for pharmaceutical products. At the time of Tiquizium Bromide 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 Tiquizium Bromide suppliers with JDMF on PharmaCompass.
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