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