from 4 to 360h flexible workload
certificate valid 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'll learn to identify indications, set up in vitro and in vivo experiments, develop solid PK/PD and toxicology data, ready IND/CTA and NDA/MAA applications, organise effective clinical trials, and handle risk, quality, and lifecycle plans for approval success.
Elevify advantages
Develop skills
- Translational drug design: quickly connect target biology to choosing the 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 results.
- Clinical trial planning: create efficient Phase I–III studies for anti-inflammatory drugs.
- Risk and lifecycle strategy: develop PV, risk management plans, and paths for growth after approval.
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 workload.What our students say
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