01 1SperaNexus Inc.
02 1Yashiro Pharmaceutical Co., Ltd.
01 2Next gallic acid bismuth
01 1Japan
02 1Blank
Registration Number : 217MF10033
Registrant's Address : 4-8-2 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-05-20
Latest Date of Registration : 2006-09-22
Registration Number : 218MF10240
Registrant's Address : 10-2 Yoshida Shimojima, Higashiosaka City, Osaka Prefecture
Initial Date of Registration : 2006-02-16
Latest Date of Registration : 2010-03-23
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PharmaCompass offers a list of Bismuth Subgallate 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 Bismuth Subgallate manufacturer or Bismuth Subgallate supplier for your needs.
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PharmaCompass also assists you with knowing the Bismuth Subgallate API Price utilized in the formulation of products. Bismuth Subgallate API Price is not always fixed or binding as the Bismuth Subgallate Price is obtained through a variety of data sources. The Bismuth Subgallate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Bismuth subgallas manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bismuth subgallas, including repackagers and relabelers. The FDA regulates Bismuth subgallas manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bismuth subgallas API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Bismuth subgallas supplier is an individual or a company that provides Bismuth subgallas active pharmaceutical ingredient (API) or Bismuth subgallas finished formulations upon request. The Bismuth subgallas suppliers may include Bismuth subgallas API manufacturers, exporters, distributors and traders.
click here to find a list of Bismuth subgallas 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 Bismuth subgallas Drug Master File in Japan (Bismuth subgallas JDMF) empowers Bismuth subgallas 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 Bismuth subgallas JDMF during the approval evaluation for pharmaceutical products. At the time of Bismuth subgallas JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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