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.
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A C10H11F3N2O5 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C10H11F3N2O5, including repackagers and relabelers. The FDA regulates C10H11F3N2O5 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C10H11F3N2O5 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 C10H11F3N2O5 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A C10H11F3N2O5 supplier is an individual or a company that provides C10H11F3N2O5 active pharmaceutical ingredient (API) or C10H11F3N2O5 finished formulations upon request. The C10H11F3N2O5 suppliers may include C10H11F3N2O5 API manufacturers, exporters, distributors and traders.
click here to find a list of C10H11F3N2O5 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 C10H11F3N2O5 Drug Master File in Korea (C10H11F3N2O5 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of C10H11F3N2O5. The MFDS reviews the C10H11F3N2O5 KDMF as part of the drug registration process and uses the information provided in the C10H11F3N2O5 KDMF to evaluate the safety and efficacy of the drug.
After submitting a C10H11F3N2O5 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 C10H11F3N2O5 API can apply through the Korea Drug Master File (KDMF).
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