from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
This Drug Development Course provides a clear, practical guide from selecting targets to ensuring safety after approval for small-molecule drugs. You will learn to identify indications, plan in vitro and in vivo studies, develop strong PK/PD and toxicology data, prepare IND/CTA and NDA/MAA applications, organise effective clinical trials, and handle risk, quality, and lifecycle plans for successful approval.
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 workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workloadWhat our students say
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