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What you will learn

• Understand how drug-target interactions influence biological activity and therapeutic outcomes.
• Analyze ADME properties and calculate key pharmacokinetic parameters from concentration-time data.
• Compare in vitro, in silico, and in vivo techniques for evaluating drug efficacy and safety.
• Interpret dose-response curves and identify pharmacodynamic relationships.
• Assess how PK and PD data are combined to predict human dosing.
• Describe the design and purpose of preclinical safety studies in regulatory drug development.
• Evaluate toxicology data to determine safe starting doses for clinical trials.
• Anticipate risks related to off-target activity, drug-drug interactions, and metabolic liabilities.
• Apply a systematic framework for advancing drug candidates toward human testing.