01 1Shiono Finesse Co., Ltd.
01 1Isoproterenol hydrochloride
01 1Japan
Registration Number : 220MF10065
Registrant's Address : Osaka Prefecture, Osaka City, Chuo Ward, Doshomachi 3-1-6
Initial Date of Registration : 2008-02-25
Latest Date of Registration : 2008-02-25
A Isoproterenol Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Isoproterenol Hydrochloride, including repackagers and relabelers. The FDA regulates Isoproterenol Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Isoproterenol Hydrochloride 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 Isoproterenol Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Isoproterenol Hydrochloride supplier is an individual or a company that provides Isoproterenol Hydrochloride active pharmaceutical ingredient (API) or Isoproterenol Hydrochloride finished formulations upon request. The Isoproterenol Hydrochloride suppliers may include Isoproterenol Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Isoproterenol Hydrochloride 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 Isoproterenol Hydrochloride Drug Master File in Japan (Isoproterenol Hydrochloride JDMF) empowers Isoproterenol Hydrochloride 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 Isoproterenol Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Isoproterenol Hydrochloride 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 Isoproterenol Hydrochloride suppliers with JDMF on PharmaCompass.
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