General characterization
  • Phase analysis: XRD. Raman. IR
  • Powder properties: particle size
  • moisture content
  • moisture adsorption
Method development and validation of qualitative, quantitative, and limit tests
  • HPLC method development and validation
  • Ion chromatography method development and validation
  • Crystallinity of API and phase impurity analysis of API
  • Phase identification and quantification of API in drug products
  • Particle size distribution method development and validation
Compound structure confirmation
  • Single crystal preparation and structural analysis
  • Infrared and Raman spectroscopy
  • NMR and Mass spectral structural analysis
Quality control
  • Identify the cause of quality problems
  • Provide solutions to quality issues