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