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Vaccine Research and Development Course

Vaccine Research and Development Course
flexible workload from 4 to 360h
valid certificate in your country

What will I learn?

This course offers a clear, hands-on guide to creating and improving mRNA vaccines for RSV-type respiratory viruses. You will cover preclinical study planning, immunogenicity and safety testing, GLP/GCP connections, and Phase I/II trial preparation. Build expertise in ethics, regulatory filings, pharmacovigilance, data handling, and team documentation for effective, compliant vaccine projects.

Elevify advantages

Develop skills

  • Design mRNA vaccines by planning constructs, LNPs, and GMP production.
  • Conduct immunogenicity assays including ELISA, neutralisation, ELISpot, and flow cytometry.
  • Plan preclinical studies by selecting models, toxicity assessment, and decision criteria.
  • Prepare regulatory documents covering IB, ethics, pharmacovigilance, and GCP compliance.
  • Collaborate on Phase I/II trials with focus on endpoints, dosing, safety, and sampling.

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

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

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