Drug Development Course
This course offers a comprehensive guide to drug development, covering everything from initial target selection to post-approval strategies for small-molecule drugs, with a focus on practical skills in regulatory submissions, clinical trials, and risk management.

4 to 360 hours of flexible workload
certificate valid in your country
What Will I Learn?
This Drug Development Course provides a clear, practical roadmap from target selection to post-approval safety for a small-molecule candidate. Learn how to define indications, design in vitro and in vivo studies, build robust PK/PD and toxicology packages, prepare IND/CTA and NDA/MAA submissions, plan efficient clinical trials, and manage risk, quality, and lifecycle strategies for successful approval.
Elevify Advantages
Develop Skills
- Translational drug design: rapidly link target biology to dosage form choice.
- Regulatory dossier skills: build sharp IND, NDA and EMA-ready submissions.
- Practical DMPK and safety: run, interpret and optimize in vitro and in vivo data.
- Clinical trial planning: design efficient Phase I–III studies for inflammatory drugs.
- Risk and lifecycle strategy: craft PV, risk plans and post-approval growth paths.
Suggested Summary
Before starting, you can change the chapters and the workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workload.What our students say
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