Farmhispania Group, a leading European CDMO in HPAPI Technologies & High Potency Fermentation.
01 1Farmhispania S. A.
02 1Curia New York, Inc.
03 1HUZHOU ZHANWANG PHARMACEUTICAL CO. ,LTD
01 3Milrinone
01 1China
02 1Spain
03 1U.S.A
Farmhispania Group, a leading European CDMO in HPAPI Technologies & High Potency Fermentation.
Registration Number : 219MF10138
Registrant's Address : Balmes 85, Atico, 08008 (Barcelona), Spain
Initial Date of Registration : 2007-04-18
Latest Date of Registration : 2007-04-18
Registration Number : 218MF10288
Registrant's Address : 33, Riverside Avenue Rensselaer, New York 12144-USA
Initial Date of Registration : 2006-02-28
Latest Date of Registration : 2014-11-17
Registration Number : 218MF10721
Registrant's Address : West Development Area, Linghu Town, Huzhou City, 313018, Zhejiang Province, China
Initial Date of Registration : 2006-09-06
Latest Date of Registration : 2019-01-21
A Milrinone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Milrinone, including repackagers and relabelers. The FDA regulates Milrinone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Milrinone 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 Milrinone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Milrinone supplier is an individual or a company that provides Milrinone active pharmaceutical ingredient (API) or Milrinone finished formulations upon request. The Milrinone suppliers may include Milrinone API manufacturers, exporters, distributors and traders.
click here to find a list of Milrinone 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 Milrinone Drug Master File in Japan (Milrinone JDMF) empowers Milrinone 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 Milrinone JDMF during the approval evaluation for pharmaceutical products. At the time of Milrinone 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 Milrinone suppliers with JDMF on PharmaCompass.
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