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