| Contents Notes |
"This concise guide delineates specific approaches to the successful development, optimization, and validation of high-quality HPLC-based analytical methods - demonstrating how these steps can be integrated into a formal process reflecting present United States Pharmacopeia (USP) regulations and International Conference on Harmonization (ICH) contributions." "Supplemented with an up-to-date bibliography, tables, and drawings, this convenient handbook is useful for analytical chemists and biochemists, pharmaceutical development chemists, pharmacologists, pharmacokineticists, laboratory and validation managers, and graduate-level students in these disciplines."--Jacket. |
