Pharmaceutical Analysis


Analytical methods needed to be validated to provide reliable data for regulatory submissions. These methods are important for a number of purposes, including testing for QC release, testing of stability samples, testing of reference materials and to provide data to support specifications. It provides a comprehensive exposure of method development and validation requirements to progress a pharmaceutical compound, at each stage of product development.

  • Electroanalytical methods
  • Mass Spectrometry
  • Titrimetry
  • Gravimetric analysis
  • Chromatography techniques
  • Spectroscopy (UV, Mass Spectroscopy, NMR)

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