01 1Shiono Finesse Co., Ltd.
01 1bepridil hydrochloride hydrate
01 1Japan
Bepridil hydrochloride hydrate
Registration Number : 304MF10114
Registrant's Address : Osaka Prefecture, Osaka City, Chuo Ward, Doshomachi 3-1-6
Initial Date of Registration : 2022-08-03
Latest Date of Registration : 2022-08-03
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PharmaCompass offers a list of Bepridil 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 Bepridil manufacturer or Bepridil supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Bepridil manufacturer or Bepridil supplier.
PharmaCompass also assists you with knowing the Bepridil API Price utilized in the formulation of products. Bepridil API Price is not always fixed or binding as the Bepridil Price is obtained through a variety of data sources. The Bepridil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cordium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cordium, including repackagers and relabelers. The FDA regulates Cordium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cordium 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 Cordium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cordium supplier is an individual or a company that provides Cordium active pharmaceutical ingredient (API) or Cordium finished formulations upon request. The Cordium suppliers may include Cordium API manufacturers, exporters, distributors and traders.
click here to find a list of Cordium 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 Cordium Drug Master File in Japan (Cordium JDMF) empowers Cordium 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 Cordium JDMF during the approval evaluation for pharmaceutical products. At the time of Cordium 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 Cordium suppliers with JDMF on PharmaCompass.
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