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PharmaCompass offers a list of Dipotassium 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 Dipotassium Glycyrrhizinate manufacturer or Dipotassium Glycyrrhizinate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dipotassium Glycyrrhizinate manufacturer or Dipotassium Glycyrrhizinate supplier.
PharmaCompass also assists you with knowing the Dipotassium Glycyrrhizinate API Price utilized in the formulation of products. Dipotassium Glycyrrhizinate API Price is not always fixed or binding as the Dipotassium Glycyrrhizinate Price is obtained through a variety of data sources. The Dipotassium Glycyrrhizinate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Glycyrrhizic Acid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glycyrrhizic Acid, including repackagers and relabelers. The FDA regulates Glycyrrhizic Acid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glycyrrhizic Acid 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 Glycyrrhizic Acid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glycyrrhizic Acid supplier is an individual or a company that provides Glycyrrhizic Acid active pharmaceutical ingredient (API) or Glycyrrhizic Acid finished formulations upon request. The Glycyrrhizic Acid suppliers may include Glycyrrhizic Acid API manufacturers, exporters, distributors and traders.
click here to find a list of Glycyrrhizic Acid 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 Glycyrrhizic Acid Drug Master File in Japan (Glycyrrhizic Acid JDMF) empowers Glycyrrhizic Acid 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 Glycyrrhizic Acid JDMF during the approval evaluation for pharmaceutical products. At the time of Glycyrrhizic Acid 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 Glycyrrhizic Acid suppliers with JDMF on PharmaCompass.
Glycyrrhizic Acid Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of Glycyrrhizic Acid GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Glycyrrhizic Acid GMP manufacturer or Glycyrrhizic Acid GMP API supplier for your needs.
A Glycyrrhizic Acid CoA (Certificate of Analysis) is a formal document that attests to Glycyrrhizic Acid's compliance with Glycyrrhizic Acid specifications and serves as a tool for batch-level quality control.
Glycyrrhizic Acid CoA mostly includes findings from lab analyses of a specific batch. For each Glycyrrhizic Acid CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
Glycyrrhizic Acid may be tested according to a variety of international standards, such as European Pharmacopoeia (Glycyrrhizic Acid EP), Glycyrrhizic Acid JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Glycyrrhizic Acid USP).