EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI Hungary Ltd.
02 1YS Life Science Co. , Ltd.
01 2Alprostadil
01 1France
02 1South Korea
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registration Number : 220MF10064
Registrant's Address : To(´) utca 1-5. , 1045 Budapest, Hungary
Initial Date of Registration : 2008-02-25
Latest Date of Registration : 2016-12-20
Registration Number : 306MF10135
Registrant's Address : 207, Sujeong-ro, Jangan-myeon, Hwaseong-si, Gyeonggi-do, 18581, Republic of Korea
Initial Date of Registration : 2024-10-16
Latest Date of Registration : 2024-10-16
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PharmaCompass offers a list of Alprostadil 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 Alprostadil manufacturer or Alprostadil supplier for your needs.
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PharmaCompass also assists you with knowing the Alprostadil API Price utilized in the formulation of products. Alprostadil API Price is not always fixed or binding as the Alprostadil Price is obtained through a variety of data sources. The Alprostadil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Prostaglandin E1;Edex;Muse;Liprostin;Caverject manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prostaglandin E1;Edex;Muse;Liprostin;Caverject, including repackagers and relabelers. The FDA regulates Prostaglandin E1;Edex;Muse;Liprostin;Caverject manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prostaglandin E1;Edex;Muse;Liprostin;Caverject 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 Prostaglandin E1;Edex;Muse;Liprostin;Caverject manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Prostaglandin E1;Edex;Muse;Liprostin;Caverject supplier is an individual or a company that provides Prostaglandin E1;Edex;Muse;Liprostin;Caverject active pharmaceutical ingredient (API) or Prostaglandin E1;Edex;Muse;Liprostin;Caverject finished formulations upon request. The Prostaglandin E1;Edex;Muse;Liprostin;Caverject suppliers may include Prostaglandin E1;Edex;Muse;Liprostin;Caverject API manufacturers, exporters, distributors and traders.
click here to find a list of Prostaglandin E1;Edex;Muse;Liprostin;Caverject 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 Prostaglandin E1;Edex;Muse;Liprostin;Caverject Drug Master File in Japan (Prostaglandin E1;Edex;Muse;Liprostin;Caverject JDMF) empowers Prostaglandin E1;Edex;Muse;Liprostin;Caverject 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 Prostaglandin E1;Edex;Muse;Liprostin;Caverject JDMF during the approval evaluation for pharmaceutical products. At the time of Prostaglandin E1;Edex;Muse;Liprostin;Caverject 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 Prostaglandin E1;Edex;Muse;Liprostin;Caverject suppliers with JDMF on PharmaCompass.
We have 2 companies offering Prostaglandin E1;Edex;Muse;Liprostin;Caverject
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