01 1Yashiro Pharmaceutical Co., Ltd.
01 1Next bismuth nitrate
01 1Blank
Registration Number : 218MF10239
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 also assists you with knowing the Bismuth Nitrate API Price utilized in the formulation of products. Bismuth Nitrate API Price is not always fixed or binding as the Bismuth Nitrate Price is obtained through a variety of data sources. The Bismuth Nitrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A BISMUTH SUBNITRATE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of BISMUTH SUBNITRATE, including repackagers and relabelers. The FDA regulates BISMUTH SUBNITRATE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. BISMUTH SUBNITRATE 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 SUBNITRATE supplier is an individual or a company that provides BISMUTH SUBNITRATE active pharmaceutical ingredient (API) or BISMUTH SUBNITRATE finished formulations upon request. The BISMUTH SUBNITRATE suppliers may include BISMUTH SUBNITRATE API manufacturers, exporters, distributors and traders.
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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 SUBNITRATE Drug Master File in Japan (BISMUTH SUBNITRATE JDMF) empowers BISMUTH SUBNITRATE 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 SUBNITRATE JDMF during the approval evaluation for pharmaceutical products. At the time of BISMUTH SUBNITRATE 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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