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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)
02 Curia Spain S. A. U. (1)
01 Hydrocortisone Sodium Phosphate (1)
02 Hydrocortisone phosphate ester sodium (1)
01 France (1)
02 U.S.A (1)
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PharmaCompass offers a list of Hydrocortisone Sodium Phosphate 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 Hydrocortisone Sodium Phosphate manufacturer or Hydrocortisone Sodium Phosphate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hydrocortisone Sodium Phosphate manufacturer or Hydrocortisone Sodium Phosphate supplier.
PharmaCompass also assists you with knowing the Hydrocortisone Sodium Phosphate API Price utilized in the formulation of products. Hydrocortisone Sodium Phosphate API Price is not always fixed or binding as the Hydrocortisone Sodium Phosphate Price is obtained through a variety of data sources. The Hydrocortisone Sodium Phosphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 0388G963HY manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 0388G963HY, including repackagers and relabelers. The FDA regulates 0388G963HY manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 0388G963HY 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 0388G963HY manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 0388G963HY supplier is an individual or a company that provides 0388G963HY active pharmaceutical ingredient (API) or 0388G963HY finished formulations upon request. The 0388G963HY suppliers may include 0388G963HY API manufacturers, exporters, distributors and traders.
click here to find a list of 0388G963HY 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 0388G963HY Drug Master File in Japan (0388G963HY JDMF) empowers 0388G963HY 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 0388G963HY JDMF during the approval evaluation for pharmaceutical products. At the time of 0388G963HY 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 0388G963HY suppliers with JDMF on PharmaCompass.
