EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI Hungary Ltd.
02 1(주)와이에스생명과학
01 1(주)와이에스생명과학
02 1Samoh Pharmaceutical Co., Ltd.
01 2Alprostadil
01 1France
02 1South Korea
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registrant Name : Samoh Pharmaceutical Co., Ltd.
Registration Date : 2023-02-02
Registration Number : 20230202-210-J-1440
Manufacturer Name : EUROAPI Hungary Ltd.
Manufacturer Address : To utca 1-5., Budapest, 1045, Hungary
Registrant Name : (주)와이에스생명과학
Registration Date : 2024-02-06
Registration Number : 20240206-210-J-1611
Manufacturer Name : (주)와이에스생명과...
Manufacturer Address : 경기도 화성시 장안면 수정로 207
38
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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Alprostadil manufacturer or Alprostadil supplier.
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 FemLife manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of FemLife, including repackagers and relabelers. The FDA regulates FemLife manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. FemLife 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 FemLife manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A FemLife supplier is an individual or a company that provides FemLife active pharmaceutical ingredient (API) or FemLife finished formulations upon request. The FemLife suppliers may include FemLife API manufacturers, exporters, distributors and traders.
click here to find a list of FemLife suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a FemLife Drug Master File in Korea (FemLife KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of FemLife. The MFDS reviews the FemLife KDMF as part of the drug registration process and uses the information provided in the FemLife KDMF to evaluate the safety and efficacy of the drug.
After submitting a FemLife KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their FemLife API can apply through the Korea Drug Master File (KDMF).
click here to find a list of FemLife suppliers with KDMF on PharmaCompass.
We have 2 companies offering FemLife
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