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01 JW Pharmaceutical Corporation (1)
02 Sekisui Medical Co., Ltd. (1)
01 Anagliptin (2)
01 Japan (1)
02 South Korea (1)
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PharmaCompass offers a list of Anagliptin 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 Anagliptin manufacturer or Anagliptin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Anagliptin manufacturer or Anagliptin supplier.
PharmaCompass also assists you with knowing the Anagliptin API Price utilized in the formulation of products. Anagliptin API Price is not always fixed or binding as the Anagliptin Price is obtained through a variety of data sources. The Anagliptin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Anagliptin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Anagliptin, including repackagers and relabelers. The FDA regulates Anagliptin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Anagliptin 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 Anagliptin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Anagliptin supplier is an individual or a company that provides Anagliptin active pharmaceutical ingredient (API) or Anagliptin finished formulations upon request. The Anagliptin suppliers may include Anagliptin API manufacturers, exporters, distributors and traders.
click here to find a list of Anagliptin 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 Anagliptin Drug Master File in Japan (Anagliptin JDMF) empowers Anagliptin 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 Anagliptin JDMF during the approval evaluation for pharmaceutical products. At the time of Anagliptin 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 Anagliptin suppliers with JDMF on PharmaCompass.
We have 2 companies offering Anagliptin
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