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PharmaCompass offers a list of L-Glutamine 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 L-Glutamine manufacturer or L-Glutamine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred L-Glutamine manufacturer or L-Glutamine supplier.
PharmaCompass also assists you with knowing the L-Glutamine API Price utilized in the formulation of products. L-Glutamine API Price is not always fixed or binding as the L-Glutamine Price is obtained through a variety of data sources. The L-Glutamine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Glutamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glutamine, including repackagers and relabelers. The FDA regulates Glutamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glutamine 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 Glutamine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glutamine supplier is an individual or a company that provides Glutamine active pharmaceutical ingredient (API) or Glutamine finished formulations upon request. The Glutamine suppliers may include Glutamine API manufacturers, exporters, distributors and traders.
click here to find a list of Glutamine 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 Glutamine Drug Master File in Japan (Glutamine JDMF) empowers Glutamine 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 Glutamine JDMF during the approval evaluation for pharmaceutical products. At the time of Glutamine 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 Glutamine suppliers with JDMF on PharmaCompass.
We have 5 companies offering Glutamine
Get in contact with the supplier of your choice: