flexible workload from 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, set up lab and animal tests, compile 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 drugs treating inflammation.
- 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 workload.What our students say
FAQs
Who is Elevify? How does it work?
Do the courses have certificates?
Are the courses free?
What is the course workload?
What are the courses like?
How do the courses work?
What is the duration of the courses?
What is the cost or price of the courses?
What is an EAD or online course and how does it work?
PDF Course
