01 1Apitoria Pharma Private Limited (Unit-I)
01 1Clasia Co., Ltd.
01 1Tripleluridin
01 1India
Registrant Name : Clasia 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...
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PharmaCompass offers a list of Trifluridine 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 Trifluridine manufacturer or Trifluridine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Trifluridine manufacturer or Trifluridine supplier.
A 5-Trifluorothymidine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 5-Trifluorothymidine, including repackagers and relabelers. The FDA regulates 5-Trifluorothymidine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 5-Trifluorothymidine 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 5-Trifluorothymidine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A 5-Trifluorothymidine supplier is an individual or a company that provides 5-Trifluorothymidine active pharmaceutical ingredient (API) or 5-Trifluorothymidine finished formulations upon request. The 5-Trifluorothymidine suppliers may include 5-Trifluorothymidine API manufacturers, exporters, distributors and traders.
click here to find a list of 5-Trifluorothymidine 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 5-Trifluorothymidine Drug Master File in Korea (5-Trifluorothymidine KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 5-Trifluorothymidine. The MFDS reviews the 5-Trifluorothymidine KDMF as part of the drug registration process and uses the information provided in the 5-Trifluorothymidine KDMF to evaluate the safety and efficacy of the drug.
After submitting a 5-Trifluorothymidine 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 5-Trifluorothymidine API can apply through the Korea Drug Master File (KDMF).
click here to find a list of 5-Trifluorothymidine suppliers with KDMF on PharmaCompass.
We have 1 companies offering 5-Trifluorothymidine
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