EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI Hungary Ltd.
01 1Ferring Korea Co., Ltd.
01 1Dinoprostone
01 1France
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registrant Name : Ferring Korea Co., Ltd.
Registration Date : 2022-11-02
Registration Number : 20221102-209-J-1396
Manufacturer Name : EUROAPI Hungary Ltd.
Manufacturer Address : To u. 1-5., Budapest, 1045, Hungary
40
PharmaCompass offers a list of Dinoprostone API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Dinoprostone manufacturer or Dinoprostone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dinoprostone manufacturer or Dinoprostone supplier.
A PGE2 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PGE2, including repackagers and relabelers. The FDA regulates PGE2 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PGE2 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 PGE2 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A PGE2 supplier is an individual or a company that provides PGE2 active pharmaceutical ingredient (API) or PGE2 finished formulations upon request. The PGE2 suppliers may include PGE2 API manufacturers, exporters, distributors and traders.
click here to find a list of PGE2 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 PGE2 Drug Master File in Korea (PGE2 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of PGE2. The MFDS reviews the PGE2 KDMF as part of the drug registration process and uses the information provided in the PGE2 KDMF to evaluate the safety and efficacy of the drug.
After submitting a PGE2 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 PGE2 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of PGE2 suppliers with KDMF on PharmaCompass.
