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PharmaCompass offers a list of Dabigatran Etexilate Mesylate 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 Dabigatran Etexilate Mesylate manufacturer or Dabigatran Etexilate Mesylate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dabigatran Etexilate Mesylate manufacturer or Dabigatran Etexilate Mesylate supplier.
PharmaCompass also assists you with knowing the Dabigatran Etexilate Mesylate API Price utilized in the formulation of products. Dabigatran Etexilate Mesylate API Price is not always fixed or binding as the Dabigatran Etexilate Mesylate Price is obtained through a variety of data sources. The Dabigatran Etexilate Mesylate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Pradaxa manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pradaxa, including repackagers and relabelers. The FDA regulates Pradaxa manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pradaxa 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 Pradaxa manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pradaxa supplier is an individual or a company that provides Pradaxa active pharmaceutical ingredient (API) or Pradaxa finished formulations upon request. The Pradaxa suppliers may include Pradaxa API manufacturers, exporters, distributors and traders.
click here to find a list of Pradaxa 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 Pradaxa Drug Master File in Korea (Pradaxa KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Pradaxa. The MFDS reviews the Pradaxa KDMF as part of the drug registration process and uses the information provided in the Pradaxa KDMF to evaluate the safety and efficacy of the drug.
After submitting a Pradaxa 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 Pradaxa API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Pradaxa suppliers with KDMF on PharmaCompass.
We have 14 companies offering Pradaxa
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