flexible workload of 4 to 360h
valid certificate in your country
What will I learn?
This Drug Development Course provides a straightforward, hands-on guide from selecting targets to ensuring safety after approval for a small-molecule drug. You will learn to identify suitable conditions, plan lab and animal tests, develop strong pharmacokinetic/pharmacodynamic and toxicology reports, ready IND/CTA and NDA/MAA applications, organise effective clinical trials, and handle risks, quality, and ongoing management for successful market entry.
Elevify advantages
Develop skills
- Translational drug design: quickly connect target biology to choosing the right dosage form.
- Regulatory dossier skills: prepare precise IND, NDA, and EMA-compliant submissions.
- Practical DMPK and safety: conduct, analyse, and improve in vitro and in vivo data.
- Clinical trial planning: create efficient Phase I–III studies for anti-inflammatory drugs.
- Risk and lifecycle strategy: develop pharmacovigilance, risk management, and post-approval expansion plans.
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 workloadWhat our students say
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