Pharmaceutical Analysis

Analytical methods must be validated to provide reliable data for regulatory presentations. These methods are essential for a number of purposes, including testing for CC release, stability sample testing, testing of reference materials and for providing data to support specifications. It provides comprehensive coverage of the development of methods and validation requirements to progress in a pharmaceutical compound, at each stage of product development.

It is estimated that the global revenues of advanced drug administration systems will be $ 151.3 billion in 2013. In 2018, it is estimated that revenues will reach almost $ 173.8 billion, which shows a compound annual growth rate (CAGR) ) of 2.8%. Europe contributed about 27% of the total drug delivery market in 2010 and was $ 36 billion. BCC expects this market to grow to $ 49 billion in 2016 at a compound annual rate of 5.6%. The global generic sector reached $ 269.8 billion in 2012. This sector is expected to reach $ 300.9 billion in 2013 and $ 518.5 billion in 2018, with a compound annual growth rate (CAGR) of 11.5%.

  • Various Separation Techniques
  • Electroanalytical methods: Potentiometry and voltammetry
  • Spectroscopy: UV, Mass Spectroscopy and other Spectroscopies techniques
  • NMR Spectroscopy
  • Chromatography techniques
  • Radioanalytical chemistry
  • Gravimetric analysis
  • UPLC and HPLC
  • Titrimetry and X-ray Crystallography
  • Mass Spectrometry

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