01 1CARBOGEN AMCIS AG
01 1Takeda Pharmaceutical Korea
01 1Maribavir
01 1Switzerland
Registrant Name : Takeda Pharmaceutical Korea
Registration Date : 2023-07-12
Registration Number : 20230712-211-J-1519
Manufacturer Name : CARBOGEN AMCIS AG
Manufacturer Address : Hauptstrasse 145 and 171, 4416 Bubendorf, Switzerland
41
PharmaCompass offers a list of Maribavir API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Maribavir manufacturer or Maribavir supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Maribavir manufacturer or Maribavir supplier.
A Maribavir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Maribavir, including repackagers and relabelers. The FDA regulates Maribavir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Maribavir 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 Maribavir manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Maribavir supplier is an individual or a company that provides Maribavir active pharmaceutical ingredient (API) or Maribavir finished formulations upon request. The Maribavir suppliers may include Maribavir API manufacturers, exporters, distributors and traders.
click here to find a list of Maribavir suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Maribavir Drug Master File in Korea (Maribavir KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Maribavir. The MFDS reviews the Maribavir KDMF as part of the drug registration process and uses the information provided in the Maribavir KDMF to evaluate the safety and efficacy of the drug.
After submitting a Maribavir 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 Maribavir API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Maribavir suppliers with KDMF on PharmaCompass.
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