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Drug Development Course

Drug Development Course
from 4 to 360h flexible workload
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

  • Translational drug design: swiftly connect target biology to optimal dosage forms.
  • Regulatory dossier expertise: prepare precise IND, NDA, and EMA-compliant submissions.
  • DMPK and safety proficiency: conduct, analyse, and refine in vitro and in vivo studies.
  • Clinical trial strategy: develop effective Phase I-III trials for inflammatory conditions.
  • Risk and lifecycle management: formulate pharmacovigilance, risk mitigation, and post-approval expansion strategies.

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.
Workload: between 4 and 360 hours

What our students say

Your lessons are perfect. I purchased the one-year package and finally have the opportunity to follow various topics of my interest without needing to change platforms... I thank you for everything you do, I've already recommended you to other people...
Giulio Carlo
Giulio CarloDigital Marketing Student
I like how the lessons are straight to the point and how I can change chapters and skip content I don't need.
Mariana Ferres
Mariana FerresPhotography Student
I like the content and the way videos are presented and transcribed, which speeds up the process!
Luciana Alvarenga
Luciana AlvarengaNail Design Student
The platform is fast, simple to use. The diversity of content and complementary videos help a lot with learning.
André Felipe
André FelipePrompt Engineering Student

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