01 1Airgas Therapeutics, LLC
01 1Braco Imaging Korea Ltd.
01 1Sulphahexafluoride
01 1U.S.A
Registrant Name : Braco Imaging Korea Ltd.
Registration Date : 2005-06-14
Registration Number : Number 267-1-ND
Manufacturer Name : Airgas Therapeutics, LLC
Manufacturer Address : 6141 Easton Road-Building 3, Plumsteadville, PA 18949-0310
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PharmaCompass offers a list of Sulfur Hexafluoride 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 Sulfur Hexafluoride manufacturer or Sulfur Hexafluoride supplier for your needs.
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PharmaCompass also assists you with knowing the Sulfur Hexafluoride API Price utilized in the formulation of products. Sulfur Hexafluoride API Price is not always fixed or binding as the Sulfur Hexafluoride Price is obtained through a variety of data sources. The Sulfur Hexafluoride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A EINECS 219-854-2 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of EINECS 219-854-2, including repackagers and relabelers. The FDA regulates EINECS 219-854-2 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. EINECS 219-854-2 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 EINECS 219-854-2 supplier is an individual or a company that provides EINECS 219-854-2 active pharmaceutical ingredient (API) or EINECS 219-854-2 finished formulations upon request. The EINECS 219-854-2 suppliers may include EINECS 219-854-2 API manufacturers, exporters, distributors and traders.
click here to find a list of EINECS 219-854-2 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 EINECS 219-854-2 Drug Master File in Korea (EINECS 219-854-2 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of EINECS 219-854-2. The MFDS reviews the EINECS 219-854-2 KDMF as part of the drug registration process and uses the information provided in the EINECS 219-854-2 KDMF to evaluate the safety and efficacy of the drug.
After submitting a EINECS 219-854-2 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 EINECS 219-854-2 API can apply through the Korea Drug Master File (KDMF).
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