With Fermion, start the journey of your innovative API.
01 3Fermion Oy
02 1Agerson Bio Co., Ltd.
03 1Emcure Pharmaceuticals Limited
04 1Gland Pharm Limited
05 1Interpretation of SA of CV
06 3Jiangsu Hengrui Pharmaceuticals Co., Ltd
07 3Joint Stock Company "Grindeks"
08 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 : 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_
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
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PharmaCompass offers a list of Dexmedetomidine Hydrochloride 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 Dexmedetomidine Hydrochloride manufacturer or Dexmedetomidine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dexmedetomidine Hydrochloride manufacturer or Dexmedetomidine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Dexmedetomidine Hydrochloride API Price utilized in the formulation of products. Dexmedetomidine Hydrochloride API Price is not always fixed or binding as the Dexmedetomidine Hydrochloride Price is obtained through a variety of data sources. The Dexmedetomidine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Precedex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Precedex, including repackagers and relabelers. The FDA regulates Precedex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Precedex 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 Precedex manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Precedex supplier is an individual or a company that provides Precedex active pharmaceutical ingredient (API) or Precedex finished formulations upon request. The Precedex suppliers may include Precedex API manufacturers, exporters, distributors and traders.
click here to find a list of Precedex 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 Precedex Drug Master File in Korea (Precedex KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Precedex. The MFDS reviews the Precedex KDMF as part of the drug registration process and uses the information provided in the Precedex KDMF to evaluate the safety and efficacy of the drug.
After submitting a Precedex 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 Precedex API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Precedex suppliers with KDMF on PharmaCompass.
We have 7 companies offering Precedex
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