EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 2EUROAPI Hungary Ltd.
02 1Newchem S. p. A.
03 1Toray Industries, Inc.
04 1YS Life Science Co. , Ltd.
01 2Beraprost Sodium
02 3Beraprost sodium
01 2France
02 1Italy
03 1Japan
04 1South Korea
Registration Number : 303MF10151
Registrant's Address : To(´) utca 1-5. , 1045 Budapest, Hungary
Initial Date of Registration : 2021-09-17
Latest Date of Registration : 2021-09-17
Registration Number : 218MF10340
Registrant's Address : To(´) utca 1-5. , 1045 Budapest, Hungary
Initial Date of Registration : 2006-03-09
Latest Date of Registration : 2012-07-09
Registration Number : 304MF10120
Registrant's Address : Via San Vittore, 39 - 20123 Milano (Italy)
Initial Date of Registration : 2022-08-17
Latest Date of Registration : 2022-08-17
Registration Number : 218MF10447
Registrant's Address : 2-1-1 Muromachi, Nihonbashi, Chuo-ku, Tokyo
Initial Date of Registration : 2006-04-27
Latest Date of Registration : 2019-03-29
Registration Number : 223MF10146
Registrant's Address : 207, Sujeong-ro, Jangan-myeon, Hwaseong-si, Gyeonggi-do, 18581, Republic of Korea
Initial Date of Registration : 2011-09-30
Latest Date of Registration : 2011-09-30
A Beraprost Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Beraprost Sodium, including repackagers and relabelers. The FDA regulates Beraprost Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Beraprost Sodium 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 Beraprost Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Beraprost Sodium supplier is an individual or a company that provides Beraprost Sodium active pharmaceutical ingredient (API) or Beraprost Sodium finished formulations upon request. The Beraprost Sodium suppliers may include Beraprost Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Beraprost Sodium 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 Beraprost Sodium Drug Master File in Japan (Beraprost Sodium JDMF) empowers Beraprost Sodium 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 Beraprost Sodium JDMF during the approval evaluation for pharmaceutical products. At the time of Beraprost Sodium 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 Beraprost Sodium suppliers with JDMF on PharmaCompass.
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