01 1Kemport Co., Ltd.
01 1Kemport Co., Ltd.
01 1Ethyl icosapentate
01 1United Kingdom
Registrant Name : Kemport Co., Ltd.
Registration Date : 2022-08-22
Registration Number : 20220822-211-J-1348
Manufacturer Name : Kemport Co., Ltd.
Manufacturer Address : Laboratory: 2nd floor, Research Building, 52, Goha-daero 719beongil, Mokpo-si, Jeolla...
66
PharmaCompass offers a list of Icosapent Ethyl 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 Icosapent Ethyl manufacturer or Icosapent Ethyl supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Icosapent Ethyl manufacturer or Icosapent Ethyl supplier.
PharmaCompass also assists you with knowing the Icosapent Ethyl API Price utilized in the formulation of products. Icosapent Ethyl API Price is not always fixed or binding as the Icosapent Ethyl Price is obtained through a variety of data sources. The Icosapent Ethyl Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A EPA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of EPA, including repackagers and relabelers. The FDA regulates EPA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. EPA 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 EPA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A EPA supplier is an individual or a company that provides EPA active pharmaceutical ingredient (API) or EPA finished formulations upon request. The EPA suppliers may include EPA API manufacturers, exporters, distributors and traders.
click here to find a list of EPA 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 EPA Drug Master File in Korea (EPA KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of EPA. The MFDS reviews the EPA KDMF as part of the drug registration process and uses the information provided in the EPA KDMF to evaluate the safety and efficacy of the drug.
After submitting a EPA 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 EPA API can apply through the Korea Drug Master File (KDMF).
click here to find a list of EPA suppliers with KDMF on PharmaCompass.
