01 2NOF Corporation
01 1Nissan cation F2-50E
02 1Nissan cation F2-50EN
01 2Japan
Registration Number : 222MF10038
Registrant's Address : 4-20-3 Ebisu, Shibuya-ku, Tokyo
Initial Date of Registration : 2010-01-28
Latest Date of Registration : 2010-01-28
Registration Number : 217MF11161
Registrant's Address : 4-20-3 Ebisu, Shibuya-ku, Tokyo
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2010-01-28
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PharmaCompass offers a list of Didecyl Dimethyl Ammonium Chloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Didecyl Dimethyl Ammonium Chloride manufacturer or Didecyl Dimethyl Ammonium Chloride supplier for your needs.
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A DIDECYLDIMETHYLAMMONIUMCHLORIDE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DIDECYLDIMETHYLAMMONIUMCHLORIDE, including repackagers and relabelers. The FDA regulates DIDECYLDIMETHYLAMMONIUMCHLORIDE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DIDECYLDIMETHYLAMMONIUMCHLORIDE 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 DIDECYLDIMETHYLAMMONIUMCHLORIDE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A DIDECYLDIMETHYLAMMONIUMCHLORIDE supplier is an individual or a company that provides DIDECYLDIMETHYLAMMONIUMCHLORIDE active pharmaceutical ingredient (API) or DIDECYLDIMETHYLAMMONIUMCHLORIDE finished formulations upon request. The DIDECYLDIMETHYLAMMONIUMCHLORIDE suppliers may include DIDECYLDIMETHYLAMMONIUMCHLORIDE API manufacturers, exporters, distributors and traders.
click here to find a list of DIDECYLDIMETHYLAMMONIUMCHLORIDE suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 DIDECYLDIMETHYLAMMONIUMCHLORIDE Drug Master File in Japan (DIDECYLDIMETHYLAMMONIUMCHLORIDE JDMF) empowers DIDECYLDIMETHYLAMMONIUMCHLORIDE 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 DIDECYLDIMETHYLAMMONIUMCHLORIDE JDMF during the approval evaluation for pharmaceutical products. At the time of DIDECYLDIMETHYLAMMONIUMCHLORIDE 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 DIDECYLDIMETHYLAMMONIUMCHLORIDE suppliers with JDMF on PharmaCompass.
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