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Drug Development Course

Drug Development Course
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.
Workload: between 4 and 360 hours

What our students say

I was just promoted to Intelligence Advisor of the Prison System, and the course from Elevify was crucial for me to be chosen.
EmersonPolice Investigator
The course was essential to meet the expectations of my boss and the company I work for.
SilviaNurse
Very great course. Lots of rich information.
WiltonCivil Firefighter

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