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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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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Potassium Iodide manufacturer or Potassium Iodide supplier.
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 Potide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Potide, including repackagers and relabelers. The FDA regulates Potide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Potide 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 Potide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Potide supplier is an individual or a company that provides Potide active pharmaceutical ingredient (API) or Potide finished formulations upon request. The Potide suppliers may include Potide API manufacturers, exporters, distributors and traders.
click here to find a list of Potide 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 Potide Drug Master File in Japan (Potide JDMF) empowers Potide 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 Potide JDMF during the approval evaluation for pharmaceutical products. At the time of Potide 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 Potide suppliers with JDMF on PharmaCompass.
