01 1Yanagishima Pharmaceutical Co., Ltd.
01 1Iodoform (production only)
01 1Blank
Iodoform (for manufacturing only)
Registration Number : 218MF10330
Registrant's Address : 1-14 Hirai 3-chome, Edogawa-ku, Tokyo
Initial Date of Registration : 2006-03-09
Latest Date of Registration : 2010-04-12
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Corporate PDF
A Iodoform manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Iodoform, including repackagers and relabelers. The FDA regulates Iodoform manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Iodoform 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 Iodoform manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Iodoform supplier is an individual or a company that provides Iodoform active pharmaceutical ingredient (API) or Iodoform finished formulations upon request. The Iodoform suppliers may include Iodoform API manufacturers, exporters, distributors and traders.
click here to find a list of Iodoform 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 Iodoform Drug Master File in Japan (Iodoform JDMF) empowers Iodoform 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 Iodoform JDMF during the approval evaluation for pharmaceutical products. At the time of Iodoform 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 Iodoform suppliers with JDMF on PharmaCompass.
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