Join us for our first Drug Development Immersion course of the new year. Learn the regulatory, commercial, and scientific factors that enable a drug to be successfully brought to market. Our industry expert presents a holistic view of preclinical and clinical development process and explains how strategic decisions made at each stage impacts subsequent stages and ultimately, the success of the approval and launch.

Appropriate for those without a science background who need a foundational understanding of the drug development process.

Ideal for anyone who works in finance, law, marketing, human resources, business development, project management, IT, administrative support, supply chain, research development, non-clinical, clinical, quality assurance, regulatory affairs, policy, government relations and manufacturing.

Past participants include:

Venture capitalists, bankers, analysts, financial managers

Insurance brokers, real estate professionals

Patient advocacy group staff, disease foundation members

Policy makers, lobbyists, attorneys

Consultants, public relations specialists, journalists

University administrators, tech transfer, research institute support staff

"This course was immensely beneficial for me. As a project manager with no pharma experience, I now feel better equipped to perform my job functions, ask insightful questions, and mitigate risks much earlier on before they become issues."

“The instructor had a simple way of explaining complex issues and topics. He tied concepts to real life examples for case studies.”