01 1Yanagishima Pharmaceutical Co., Ltd.
01 1Potassium iodide (production only)
01 1Blank
Potassium iodide (for manufacturing purposes only)
Registration Number : 218MF10333
Registrant's Address : 1-5-17 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2006-03-09
Latest Date of Registration : 2010-04-12
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PharmaCompass offers a list of Potassium 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 Potassium Iodide manufacturer or Potassium Iodide supplier for your needs.
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PharmaCompass also assists you with knowing the Potassium Iodide API Price utilized in the formulation of products. Potassium Iodide API Price is not always fixed or binding as the Potassium Iodide Price is obtained through a variety of data sources. The Potassium Iodide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Kaliumiodid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Kaliumiodid, including repackagers and relabelers. The FDA regulates Kaliumiodid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Kaliumiodid 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 Kaliumiodid supplier is an individual or a company that provides Kaliumiodid active pharmaceutical ingredient (API) or Kaliumiodid finished formulations upon request. The Kaliumiodid suppliers may include Kaliumiodid API manufacturers, exporters, distributors and traders.
click here to find a list of Kaliumiodid 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 Kaliumiodid Drug Master File in Japan (Kaliumiodid JDMF) empowers Kaliumiodid 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 Kaliumiodid JDMF during the approval evaluation for pharmaceutical products. At the time of Kaliumiodid 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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