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
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PharmaCompass offers a list of Milrinone Lactate 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 Milrinone Lactate manufacturer or Milrinone Lactate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Milrinone Lactate manufacturer or Milrinone Lactate supplier.
PharmaCompass also assists you with knowing the Milrinone Lactate API Price utilized in the formulation of products. Milrinone Lactate API Price is not always fixed or binding as the Milrinone Lactate Price is obtained through a variety of data sources. The Milrinone Lactate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Milrinone Lactate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Milrinone Lactate, including repackagers and relabelers. The FDA regulates Milrinone Lactate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Milrinone Lactate 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 Lactate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Milrinone Lactate supplier is an individual or a company that provides Milrinone Lactate active pharmaceutical ingredient (API) or Milrinone Lactate finished formulations upon request. The Milrinone Lactate suppliers may include Milrinone Lactate API manufacturers, exporters, distributors and traders.
click here to find a list of Milrinone Lactate 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 Lactate Drug Master File in Japan (Milrinone Lactate JDMF) empowers Milrinone Lactate 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 Lactate JDMF during the approval evaluation for pharmaceutical products. At the time of Milrinone Lactate 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 Lactate suppliers with JDMF on PharmaCompass.
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