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PharmaCompass offers a list of Glycrrhizin 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 Glycrrhizin manufacturer or Glycrrhizin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Glycrrhizin manufacturer or Glycrrhizin supplier.
PharmaCompass also assists you with knowing the Glycrrhizin API Price utilized in the formulation of products. Glycrrhizin API Price is not always fixed or binding as the Glycrrhizin Price is obtained through a variety of data sources. The Glycrrhizin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Glycyrhhiza Glabra manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glycyrhhiza Glabra, including repackagers and relabelers. The FDA regulates Glycyrhhiza Glabra manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glycyrhhiza Glabra 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 Glycyrhhiza Glabra manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glycyrhhiza Glabra supplier is an individual or a company that provides Glycyrhhiza Glabra active pharmaceutical ingredient (API) or Glycyrhhiza Glabra finished formulations upon request. The Glycyrhhiza Glabra suppliers may include Glycyrhhiza Glabra API manufacturers, exporters, distributors and traders.
click here to find a list of Glycyrhhiza Glabra 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 Glycyrhhiza Glabra Drug Master File in Japan (Glycyrhhiza Glabra JDMF) empowers Glycyrhhiza Glabra 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 Glycyrhhiza Glabra JDMF during the approval evaluation for pharmaceutical products. At the time of Glycyrhhiza Glabra 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 Glycyrhhiza Glabra suppliers with JDMF on PharmaCompass.
We have 2 companies offering Glycyrhhiza Glabra
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