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01 Takasago Chemical Co., Ltd. (1)
01 Hinokitiol (1)
01 Japan (1)
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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, Price,and more, enabling you to easily find the right Hinokitiol manufacturer or Hinokitiol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hinokitiol manufacturer or Hinokitiol supplier.
PharmaCompass also assists you with knowing the Hinokitiol API Price utilized in the formulation of products. Hinokitiol API Price is not always fixed or binding as the Hinokitiol Price is obtained through a variety of data sources. The Hinokitiol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
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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