01 1Takasago Chemical Co., Ltd.
01 1Hinokitiol
01 1Japan
Registration Number : 217MF10308
Registrant's Address : Nissei Aroma Square 17th Floor, 5-37-1 Kamata, Ota-ku, Tokyo
Initial Date of Registration : 2005-07-04
Latest Date of Registration : 2009-04-22
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PharmaCompass offers a list of Hinokitiol 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 Hinokitiol manufacturer or Hinokitiol supplier for your needs.
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A Hinokitol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hinokitol, including repackagers and relabelers. The FDA regulates Hinokitol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hinokitol 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 Hinokitol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Hinokitol supplier is an individual or a company that provides Hinokitol active pharmaceutical ingredient (API) or Hinokitol finished formulations upon request. The Hinokitol suppliers may include Hinokitol API manufacturers, exporters, distributors and traders.
click here to find a list of Hinokitol 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 Hinokitol Drug Master File in Japan (Hinokitol JDMF) empowers Hinokitol 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 Hinokitol JDMF during the approval evaluation for pharmaceutical products. At the time of Hinokitol 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 Hinokitol suppliers with JDMF on PharmaCompass.
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