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 Sevelamer manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sevelamer, including repackagers and relabelers. The FDA regulates Sevelamer manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sevelamer 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 Sevelamer manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sevelamer supplier is an individual or a company that provides Sevelamer active pharmaceutical ingredient (API) or Sevelamer finished formulations upon request. The Sevelamer suppliers may include Sevelamer API manufacturers, exporters, distributors and traders.
click here to find a list of Sevelamer 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 Sevelamer Drug Master File in Japan (Sevelamer JDMF) empowers Sevelamer 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 Sevelamer JDMF during the approval evaluation for pharmaceutical products. At the time of Sevelamer 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 Sevelamer suppliers with JDMF on PharmaCompass.
