Pharmaceutical dissolution testing: fundamentals and essential applications (an overview) -- Bioavailability and bioequivalence (BE): fundamentals and applications in drug product development -- Solubility, dissolution, permeability, and classification systems -- Understanding the mechanics of dissolution : mathematical models and simulations -- Dissolution testing methods: necessity is the mother of invention! -- Essentials of dissolution testing of pharmaceutical systems -- Dissolution/release test data (profile): requirements, analyses, and regulatory expectations -- Automation in dissolution testing: recent advances and continuing challenges -- In vitro - in vivo correlations (IVIVCS) : what makes them challenging! -- Biorelevant dissolution/release test method development for pharmaceutical dosage forms -- Bioavailability prediction software : hype or reality! -- Challenges and unique applications of IVIVC in drug development -- Dissolution testing in generic drug development : methods, requirements, and regulatory expectation/requirements -- Successful bioequivalence investigations : current challenges and possible solutions -- Beyond guidance(s) : convincing regulatory authorities through creative dissolution data interpretation -- Biosimilars : the emerging frontier of generics : role of dissolution testing -- Patentability of drug product based on dissolution data : intellectual property considerations! -- Setting up clinical therapeutics safety-based QC specifications for dissolution testing of a finished product -- Unlocking the mystery(ies) while predicting bioavailability from dissolution.