from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
This Drug Development Course provides a straightforward, hands-on guide from choosing targets to ensuring safety after approval for small-molecule drugs. You will learn to identify disease indications, set up lab and animal studies, develop strong pharmacokinetics/pharmacodynamics and toxicology data, prepare IND/CTA and NDA/MAA applications, organise effective clinical trials, and handle risks, quality, and long-term strategies for successful market approval.
Elevify advantages
Develop skills
- Translational drug design: quickly connect target biology to selecting 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: design cost-effective Phase I–III studies for anti-inflammatory drugs.
- Risk and lifecycle strategy: develop pharmacovigilance, risk management plans, and post-approval expansion routes.
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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