01 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
02 1MSN LABORATORIES PRIVATE LIMITED Kardanur Village IN
01 2Trifluridine
01 2India
01 2Valid
Certificate Number : CEP 2020-369 - Rev 01
Status : Valid
Issue Date : 2023-12-13
Type : Chemical
Substance Number : 2910
Certificate Number : R0-CEP 2021-202 - Rev 01
Status : Valid
Issue Date : 2023-08-10
Type : Chemical
Substance Number : 2910
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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, Price,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.
PharmaCompass also assists you with knowing the Trifluridine API Price utilized in the formulation of products. Trifluridine API Price is not always fixed or binding as the Trifluridine Price is obtained through a variety of data sources. The Trifluridine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Virophta manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Virophta, including repackagers and relabelers. The FDA regulates Virophta manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Virophta 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 Virophta manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Virophta supplier is an individual or a company that provides Virophta active pharmaceutical ingredient (API) or Virophta finished formulations upon request. The Virophta suppliers may include Virophta API manufacturers, exporters, distributors and traders.
click here to find a list of Virophta suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Virophta CEP of the European Pharmacopoeia monograph is often referred to as a Virophta Certificate of Suitability (COS). The purpose of a Virophta CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Virophta EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Virophta to their clients by showing that a Virophta CEP has been issued for it. The manufacturer submits a Virophta CEP (COS) as part of the market authorization procedure, and it takes on the role of a Virophta CEP holder for the record. Additionally, the data presented in the Virophta CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Virophta DMF.
A Virophta CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Virophta CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Virophta suppliers with CEP (COS) on PharmaCompass.
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