01 1M/sSionc Pharmaceuticals Pvt ltd
01 1Nelarabine IH
01 1WC-0273A3
01 1India
Date of Issue : 2021-03-25
Valid Till : 2023-05-11
Written Confirmation Number : WC-0273A3
Address of the Firm : Plot No. 34A, J.N.Pharma City, Parawada (M), Vishakhapatnam-Dist A.P
A Nelarabine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nelarabine, including repackagers and relabelers. The FDA regulates Nelarabine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nelarabine 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 Nelarabine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nelarabine supplier is an individual or a company that provides Nelarabine active pharmaceutical ingredient (API) or Nelarabine finished formulations upon request. The Nelarabine suppliers may include Nelarabine API manufacturers, exporters, distributors and traders.
click here to find a list of Nelarabine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Nelarabine written confirmation (Nelarabine WC) is an official document issued by a regulatory agency to a Nelarabine manufacturer, verifying that the manufacturing facility of a Nelarabine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Nelarabine APIs or Nelarabine finished pharmaceutical products to another nation, regulatory agencies frequently require a Nelarabine WC (written confirmation) as part of the regulatory process.
click here to find a list of Nelarabine suppliers with Written Confirmation (WC) on PharmaCompass.
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