Drug Development Course
This course equips pharmacy professionals with comprehensive knowledge on small-molecule drug development, covering target selection, DMPK studies, regulatory submissions like IND and NDA, clinical trial design, safety assessments, and lifecycle strategies to drive therapeutic innovation in real-world settings.

flexible workload of 4 to 360h
valid certificate in your country
What will I learn?
Gain a practical guide from target selection to post-approval safety for small-molecule drugs. Master defining indications, designing in vitro and in vivo studies, developing PK/PD and toxicology data, preparing IND/CTA and NDA/MAA submissions, planning clinical trials, and handling risk, quality, and lifecycle management for drug approval success.
Elevify advantages
Develop skills
- Master translational drug design linking target biology to dosage forms swiftly.
- Develop regulatory skills for preparing IND, NDA, and EMA-compliant submissions.
- Acquire practical expertise in DMPK and safety data from in vitro and in vivo studies.
- Learn to plan efficient Phase I-III clinical trials for inflammatory conditions.
- Build strategies for pharmacovigilance, risk management, and post-approval lifecycle growth.
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 workload.What our students say
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