01 1Apitoria Pharma Private Limited (Unit-I)
01 1Klasia Co., Ltd.
01 1Trifluridine
01 1India
Registrant Name : Klasia Co., Ltd.
Registration Date : 2021-11-08
Registration Number : 20211108-211-J-1051
Manufacturer Name : Apitoria Pharma Private Limi...
Manufacturer Address : Survey No. 379, 385, 386, 388 to 396, Borpatla village, Hatnoora Mandal, Sangareddy D...
A Trifluridine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trifluridine, including repackagers and relabelers. The FDA regulates Trifluridine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trifluridine 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 Trifluridine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Trifluridine supplier is an individual or a company that provides Trifluridine active pharmaceutical ingredient (API) or Trifluridine finished formulations upon request. The Trifluridine suppliers may include Trifluridine API manufacturers, exporters, distributors and traders.
click here to find a list of Trifluridine 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 Trifluridine Drug Master File in Korea (Trifluridine KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Trifluridine. The MFDS reviews the Trifluridine KDMF as part of the drug registration process and uses the information provided in the Trifluridine KDMF to evaluate the safety and efficacy of the drug.
After submitting a Trifluridine 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 Trifluridine API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Trifluridine suppliers with KDMF on PharmaCompass.
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