With Fermion, start the journey of your innovative API.
01 3Fermion Oy
02 1Emcure Pharmaceuticals Limited
03 1Gland Pharm Limited
04 1Interpretation of SA of CV
05 3Jiangsu Hengrui Pharmaceuticals Co., Ltd
06 3Joint Stock Company "Grindeks"
07 1Strem Chemical, Inc
With Fermion, start the journey of your innovative API.
Registrant Name : Korea Farm Bio Co., Ltd.
Registration Date : 2024-05-01
Registration Number : No. 5382-1-ND(2)
Manufacturer Name : Fermion Oy
Manufacturer Address : Laaketehtaantie 2. FIN-90660 Oulu
With Fermion, start the journey of your innovative API.
Registrant Name : M-Peak Korea Co., Ltd.
Registration Date : 2022-10-18
Registration Number : No. 5382-1-ND(1)
Manufacturer Name : Fermion Oy
Manufacturer Address : Laaketehtaantie 2, FI-90660 Oulu, Finland
With Fermion, start the journey of your innovative API.
Registrant Name : Korea Pfizer Pharmaceutical Co., Ltd.
Registration Date : 2010-05-27
Registration Number : Su5382-1-ND
Manufacturer Name : Fermion Oy
Manufacturer Address : Laaketehtaantie 2. FIN-90660 Oulu_x000D_
A Dexmedetomidine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dexmedetomidine, including repackagers and relabelers. The FDA regulates Dexmedetomidine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dexmedetomidine 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 Dexmedetomidine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dexmedetomidine supplier is an individual or a company that provides Dexmedetomidine active pharmaceutical ingredient (API) or Dexmedetomidine finished formulations upon request. The Dexmedetomidine suppliers may include Dexmedetomidine API manufacturers, exporters, distributors and traders.
click here to find a list of Dexmedetomidine 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 Dexmedetomidine Drug Master File in Korea (Dexmedetomidine KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Dexmedetomidine. The MFDS reviews the Dexmedetomidine KDMF as part of the drug registration process and uses the information provided in the Dexmedetomidine KDMF to evaluate the safety and efficacy of the drug.
After submitting a Dexmedetomidine 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 Dexmedetomidine API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Dexmedetomidine suppliers with KDMF on PharmaCompass.
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