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.
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A Prepidil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prepidil, including repackagers and relabelers. The FDA regulates Prepidil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prepidil 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 Prepidil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Prepidil supplier is an individual or a company that provides Prepidil active pharmaceutical ingredient (API) or Prepidil finished formulations upon request. The Prepidil suppliers may include Prepidil API manufacturers, exporters, distributors and traders.
click here to find a list of Prepidil 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 Prepidil Drug Master File in Korea (Prepidil KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Prepidil. The MFDS reviews the Prepidil KDMF as part of the drug registration process and uses the information provided in the Prepidil KDMF to evaluate the safety and efficacy of the drug.
After submitting a Prepidil 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 Prepidil API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Prepidil suppliers with KDMF on PharmaCompass.
