01 1Yanagishima Pharmaceutical Co., Ltd.
01 1Potassium iodide (production only)
01 1Blank
Potassium iodide (for manufacturing 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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A Potassium Iodide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Potassium Iodide, including repackagers and relabelers. The FDA regulates Potassium Iodide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Potassium Iodide 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 Potassium Iodide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Potassium Iodide supplier is an individual or a company that provides Potassium Iodide active pharmaceutical ingredient (API) or Potassium Iodide finished formulations upon request. The Potassium Iodide suppliers may include Potassium Iodide API manufacturers, exporters, distributors and traders.
click here to find a list of Potassium Iodide 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 Potassium Iodide Drug Master File in Japan (Potassium Iodide JDMF) empowers Potassium Iodide 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 Potassium Iodide JDMF during the approval evaluation for pharmaceutical products. At the time of Potassium Iodide 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 Potassium Iodide suppliers with JDMF on PharmaCompass.
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