01 1Kaiping Genuine Biochemical Pharmaceutical Co., Ltd.
01 1엠피크코리아(주)
01 1Adenosine triphosphate disodium
01 1China
Adenosine triphosphate disodium
Registrant Name : 엠피크코리아(주)
Registration Date : 2021-01-12
Registration Number : 20210112-210-J-311
Manufacturer Name : Kaiping Genuine Biochemical ...
Manufacturer Address : No. 1 Xinke Road, Biaohai Industrial Park, Shatang Town, Kaiping City, Guangdong, Chi...
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PharmaCompass offers a list of Adenosine Triphosphate 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 Adenosine Triphosphate manufacturer or Adenosine Triphosphate supplier for your needs.
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PharmaCompass also assists you with knowing the Adenosine Triphosphate API Price utilized in the formulation of products. Adenosine Triphosphate API Price is not always fixed or binding as the Adenosine Triphosphate Price is obtained through a variety of data sources. The Adenosine Triphosphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Fosfobion manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fosfobion, including repackagers and relabelers. The FDA regulates Fosfobion manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fosfobion 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 Fosfobion supplier is an individual or a company that provides Fosfobion active pharmaceutical ingredient (API) or Fosfobion finished formulations upon request. The Fosfobion suppliers may include Fosfobion API manufacturers, exporters, distributors and traders.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Fosfobion Drug Master File in Korea (Fosfobion KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Fosfobion. The MFDS reviews the Fosfobion KDMF as part of the drug registration process and uses the information provided in the Fosfobion KDMF to evaluate the safety and efficacy of the drug.
After submitting a Fosfobion 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 Fosfobion API can apply through the Korea Drug Master File (KDMF).
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