EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registration Number : 218MF10733
Registrant's Address : 37 Hollands Road, Haverhill, Suffolk CB9 8PU, U.S. K.
Initial Date of Registration : 2006-09-06
Latest Date of Registration : 2011-04-12
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PharmaCompass offers a list of Sevelamer Hydrochloride 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 Sevelamer Hydrochloride manufacturer or Sevelamer Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sevelamer Hydrochloride manufacturer or Sevelamer Hydrochloride supplier.
PharmaCompass also assists you with knowing the Sevelamer Hydrochloride API Price utilized in the formulation of products. Sevelamer Hydrochloride API Price is not always fixed or binding as the Sevelamer Hydrochloride Price is obtained through a variety of data sources. The Sevelamer Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A RenaGel manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of RenaGel, including repackagers and relabelers. The FDA regulates RenaGel manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. RenaGel 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 RenaGel manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A RenaGel supplier is an individual or a company that provides RenaGel active pharmaceutical ingredient (API) or RenaGel finished formulations upon request. The RenaGel suppliers may include RenaGel API manufacturers, exporters, distributors and traders.
click here to find a list of RenaGel 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 RenaGel Drug Master File in Japan (RenaGel JDMF) empowers RenaGel 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 RenaGel JDMF during the approval evaluation for pharmaceutical products. At the time of RenaGel 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 RenaGel suppliers with JDMF on PharmaCompass.
