01 1F2 Chemicals Ltd
01 1GE Healthcare AS Korea Branch
01 1perfluorobutane
01 1United Kingdom
Registrant Name : GE Healthcare AS Korea Branch
Registration Date : 2012-03-30
Registration Number : 3231-2-ND
Manufacturer Name : F2 Chemicals Ltd
Manufacturer Address : Lea Lane, Lea Town, Preston, lancashire PR4 ORZ, UK
76
PharmaCompass offers a list of Perfluorobutane 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 Perfluorobutane manufacturer or Perfluorobutane supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Perfluorobutane manufacturer or Perfluorobutane supplier.
PharmaCompass also assists you with knowing the Perfluorobutane API Price utilized in the formulation of products. Perfluorobutane API Price is not always fixed or binding as the Perfluorobutane Price is obtained through a variety of data sources. The Perfluorobutane Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CEA 410 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CEA 410, including repackagers and relabelers. The FDA regulates CEA 410 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CEA 410 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A CEA 410 supplier is an individual or a company that provides CEA 410 active pharmaceutical ingredient (API) or CEA 410 finished formulations upon request. The CEA 410 suppliers may include CEA 410 API manufacturers, exporters, distributors and traders.
click here to find a list of CEA 410 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 CEA 410 Drug Master File in Korea (CEA 410 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of CEA 410. The MFDS reviews the CEA 410 KDMF as part of the drug registration process and uses the information provided in the CEA 410 KDMF to evaluate the safety and efficacy of the drug.
After submitting a CEA 410 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 CEA 410 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of CEA 410 suppliers with KDMF on PharmaCompass.
