01 1Permakem Asia Co., Ltd.
01 1Aluminum chlorohydrate allantoinate
01 1Japan
Aluminum Chlorohydroxyallantoinate
Registration Number : 217MF10700
Registrant's Address : 1-10-11, Nihonbashi Horidomecho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-10-07
Latest Date of Registration : 2013-03-05
A Aluminium Chlorohydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aluminium Chlorohydrate, including repackagers and relabelers. The FDA regulates Aluminium Chlorohydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aluminium Chlorohydrate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Aluminium Chlorohydrate supplier is an individual or a company that provides Aluminium Chlorohydrate active pharmaceutical ingredient (API) or Aluminium Chlorohydrate finished formulations upon request. The Aluminium Chlorohydrate suppliers may include Aluminium Chlorohydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Aluminium Chlorohydrate 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 Aluminium Chlorohydrate Drug Master File in Japan (Aluminium Chlorohydrate JDMF) empowers Aluminium Chlorohydrate 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 Aluminium Chlorohydrate JDMF during the approval evaluation for pharmaceutical products. At the time of Aluminium Chlorohydrate 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 Aluminium Chlorohydrate suppliers with JDMF on PharmaCompass.
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