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