01 1Sanyo Chemical Research Institute Co., Ltd.
01 1Saxagliptin Hydrate
01 1Gabon
Registration Number : 305MF10004
Registrant's Address : 148-1 Tajii, Mihara-ku, Sakai City, Osaka Prefecture
Initial Date of Registration : 2023-01-11
Latest Date of Registration : 2023-01-11
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PharmaCompass offers a list of Saxagliptin 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 Saxagliptin manufacturer or Saxagliptin supplier for your needs.
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PharmaCompass also assists you with knowing the Saxagliptin API Price utilized in the formulation of products. Saxagliptin API Price is not always fixed or binding as the Saxagliptin Price is obtained through a variety of data sources. The Saxagliptin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Saxagliptin Hydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Saxagliptin Hydrate, including repackagers and relabelers. The FDA regulates Saxagliptin Hydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Saxagliptin Hydrate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Saxagliptin Hydrate supplier is an individual or a company that provides Saxagliptin Hydrate active pharmaceutical ingredient (API) or Saxagliptin Hydrate finished formulations upon request. The Saxagliptin Hydrate suppliers may include Saxagliptin Hydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Saxagliptin Hydrate 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 Saxagliptin Hydrate Drug Master File in Japan (Saxagliptin Hydrate JDMF) empowers Saxagliptin Hydrate 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 Saxagliptin Hydrate JDMF during the approval evaluation for pharmaceutical products. At the time of Saxagliptin Hydrate JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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