
edXPharmaceutical innovation is a complex journey shaped by economics, law, and rigorous science. This intermediate course pulls back the curtain on clinical trials, drug-target interactions, pharmacokinetics, and safety evaluation—the core disciplines that determine whether a molecule becomes a medicine.
You'll learn to calculate first-in-human doses, navigate the patent landscape that protects innovation, and apply regulatory insights that can accelerate approval for critical therapies. Real case studies drawn from published research ground each concept, showing how theory drives real-world decisions in drug development.
Analyze the economic, legal, and regulatory factors that drive pharmaceutical innovation. ,Understand the progression of clinical trials and interpret data collected at each stage. ,Apply methods for measuring and quantifying drug-target interactions and biological activity. ,Master the principles of pharmacokinetics, including ADME properties and PK/PD modeling. ,Evaluate drug safety using both in vitro and in vivo study approaches. ,Calculate appropriate first-in-human doses and predict human efficacy from preclinical data. ,Implement approaches to lead discovery and optimization for improved efficacy and safety. ,Navigate the role of patents and intellectual property in pharmaceutical development. ,Identify how regulatory designations can accelerate approval for critical therapies. ,Apply real-world insights from case studies drawn directly from the pharmaceutical research literature.
Price
No active coupon right now
Advertisement
No coupon right now. We'll tell you when there is one.
More in Science




Tracking since 1 Aug— not enough history yet to tell you whether today's price is any good. Watch the course and we'll tell you when it drops.
This is what we recorded in US pricing — not every price this course has ever had, and prices differ by country.