Impurity profiling and analysis of TheraPure GMP nucleotides

Overview


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Nucleoside triphosphates (NTPs) are vital components of emerging RNA therapeutics and vaccines. Controlling impurities that may be present in them while understanding key product quality attributes that make them suitable for good manufacturing practice (GMP) production is important for the successful development of these therapeutics and vaccines.

Download this white paper to help you recognize major impurities and identify quality attributes when looking for GMP-quality NTPs.

  • Impurity profiling and analysis of TheraPure GMP nucleotides
  • Quality and consistency of N1-methylpseudouridine triphosphate
This content is provided by Thermo Fisher Scientific - Biosciences, and any views and opinions expressed do not necessarily reflect those of Biopharma-Reporter.com

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Selecting raw materials is one of the earliest steps in the development of mRNA vaccines and therapeutics. The materials you choose have the potential to influence your process development and drug quality.

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