EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI Hungary Ltd.
01 1Korea Ferring Pharmaceutical Co., Ltd.
01 1Dinoprostone
01 1France
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registrant Name : Korea Ferring Pharmaceutical 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
61
PharmaCompass offers a list of Dinoprostone 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 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.
PharmaCompass also assists you with knowing the Dinoprostone API Price utilized in the formulation of products. Dinoprostone API Price is not always fixed or binding as the Dinoprostone Price is obtained through a variety of data sources. The Dinoprostone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A P2E manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of P2E, including repackagers and relabelers. The FDA regulates P2E manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. P2E 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 P2E manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A P2E supplier is an individual or a company that provides P2E active pharmaceutical ingredient (API) or P2E finished formulations upon request. The P2E suppliers may include P2E API manufacturers, exporters, distributors and traders.
click here to find a list of P2E 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 P2E Drug Master File in Korea (P2E KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of P2E. The MFDS reviews the P2E KDMF as part of the drug registration process and uses the information provided in the P2E KDMF to evaluate the safety and efficacy of the drug.
After submitting a P2E 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 P2E API can apply through the Korea Drug Master File (KDMF).
click here to find a list of P2E suppliers with KDMF on PharmaCompass.
