Handbook of Pharmaceutical Analysis by HPLC

Satinder Ahuja is a leading expert on water quality improvement. He earned his PhD in analytical chemistry from the University of the Sciences in Philadelphia. He worked for Novartis Corp. in various leadership positions for over 25 years and taught as an adjunct professor at Pace University for over 10 years. As president of Ahuja Consulting, he advises on water quality issues relating to chemicals and pharmaceuticals. A member of the executive committee of the Rivers of the World Foundation (ROW), Dr. Ahuja has organized numerous global symposia on improving water quality, including presentations for the American Chemical Society and UNESCO. Dr. Ahuja has published numerous papers and more than 25 books. His latest books are Contaminants in Our Water (ACS, 2020); Evaluating Water Quality to Prevent Future Disasters (Elsevier, 2019); Advances in Water Purification Techniques (Elsevier, 2019); and Chemistry and Water (Elsevier, 2017).

Key concepts of HPLC in pharmaceutical analysis HPLC instrumentation: in pharmaceutical analysis: status, advances and trends HPLC columns for pharmaceutical Sample preparation for HPLC analysis of drug products HPLC method development Validation of HPLC methods in pharmaceutical analysis Ion Chromatography How to be more successful with HPLC analysis:: practical aspects in HPLC operation Regulatory considerations in HPLC anaysis HPLC system calibration for GMP compliance System validation: pre-installation, IQ, OQ and PQ Assays and stability testing Impurity evaluation HPLC in dissolution testing Cleaning validation using HPCL for analysis LC/MS application in high throughput ADME screen Chiral separations Applications of LC/MS in pharmaceutical analysis Application of LC-MMR in Pharmaceutical Analysis Chromatography data systems (CDS) in the pharmaceutical laboratory; its history, advances and future direction New developments in HPLC