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PharmaCompass offers a list of Glycine 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 Glycine manufacturer or Glycine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Glycine manufacturer or Glycine supplier.
PharmaCompass also assists you with knowing the Glycine API Price utilized in the formulation of products. Glycine API Price is not always fixed or binding as the Glycine Price is obtained through a variety of data sources. The Glycine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Glycine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glycine, including repackagers and relabelers. The FDA regulates Glycine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glycine 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 Glycine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glycine supplier is an individual or a company that provides Glycine active pharmaceutical ingredient (API) or Glycine finished formulations upon request. The Glycine suppliers may include Glycine API manufacturers, exporters, distributors and traders.
click here to find a list of Glycine 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 Glycine Drug Master File in Japan (Glycine JDMF) empowers Glycine 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 Glycine JDMF during the approval evaluation for pharmaceutical products. At the time of Glycine 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 Glycine suppliers with JDMF on PharmaCompass.
We have 4 companies offering Glycine
Get in contact with the supplier of your choice: