01 1NOF Corporation
01 1Nissan cation M2-100
01 1Japan
Registration Number : 220MF10240
Registrant's Address : 20-3 Ebisu 4-chome, Shibuya-ku, Tokyo
Initial Date of Registration : 2008-12-04
Latest Date of Registration : 2008-12-04
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PharmaCompass offers a list of Myristalkonium Chloride 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 Myristalkonium Chloride manufacturer or Myristalkonium Chloride supplier for your needs.
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A Myristyl dimethyl benzyl ammonium chloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Myristyl dimethyl benzyl ammonium chloride, including repackagers and relabelers. The FDA regulates Myristyl dimethyl benzyl ammonium chloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Myristyl dimethyl benzyl ammonium chloride 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 Myristyl dimethyl benzyl ammonium chloride supplier is an individual or a company that provides Myristyl dimethyl benzyl ammonium chloride active pharmaceutical ingredient (API) or Myristyl dimethyl benzyl ammonium chloride finished formulations upon request. The Myristyl dimethyl benzyl ammonium chloride suppliers may include Myristyl dimethyl benzyl ammonium chloride API manufacturers, exporters, distributors and traders.
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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 Myristyl dimethyl benzyl ammonium chloride Drug Master File in Japan (Myristyl dimethyl benzyl ammonium chloride JDMF) empowers Myristyl dimethyl benzyl ammonium chloride 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 Myristyl dimethyl benzyl ammonium chloride JDMF during the approval evaluation for pharmaceutical products. At the time of Myristyl dimethyl benzyl ammonium chloride 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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