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