01 1Yanagishima Pharmaceutical Co., Ltd.
01 1Sodium iodide (production only)
01 1Blank
Sodium iodide (for manufacturing only)
Registration Number : 218MF10332
Registrant's Address : 1-14 Hirai 3-chome, Edogawa-ku, Tokyo
Initial Date of Registration : 2006-03-09
Latest Date of Registration : 2010-04-13
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PharmaCompass offers a list of Sodium Iodide 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 Sodium Iodide manufacturer or Sodium Iodide supplier for your needs.
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PharmaCompass also assists you with knowing the Sodium Iodide API Price utilized in the formulation of products. Sodium Iodide API Price is not always fixed or binding as the Sodium Iodide Price is obtained through a variety of data sources. The Sodium Iodide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A NAI manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NAI, including repackagers and relabelers. The FDA regulates NAI manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NAI 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 NAI supplier is an individual or a company that provides NAI active pharmaceutical ingredient (API) or NAI finished formulations upon request. The NAI suppliers may include NAI API manufacturers, exporters, distributors and traders.
click here to find a list of NAI 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 NAI Drug Master File in Japan (NAI JDMF) empowers NAI 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 NAI JDMF during the approval evaluation for pharmaceutical products. At the time of NAI 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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