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
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
A SODIUM IODIDE (I-123) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SODIUM IODIDE (I-123), including repackagers and relabelers. The FDA regulates SODIUM IODIDE (I-123) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SODIUM IODIDE (I-123) 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 SODIUM IODIDE (I-123) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A SODIUM IODIDE (I-123) supplier is an individual or a company that provides SODIUM IODIDE (I-123) active pharmaceutical ingredient (API) or SODIUM IODIDE (I-123) finished formulations upon request. The SODIUM IODIDE (I-123) suppliers may include SODIUM IODIDE (I-123) API manufacturers, exporters, distributors and traders.
click here to find a list of SODIUM IODIDE (I-123) 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 SODIUM IODIDE (I-123) Drug Master File in Japan (SODIUM IODIDE (I-123) JDMF) empowers SODIUM IODIDE (I-123) 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 SODIUM IODIDE (I-123) JDMF during the approval evaluation for pharmaceutical products. At the time of SODIUM IODIDE (I-123) 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 SODIUM IODIDE (I-123) suppliers with JDMF on PharmaCompass.
LOOKING FOR A SUPPLIER?
