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Vaccine Research and Development Course

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

What will I learn?

This course provides a practical guide to mRNA vaccine design and development for respiratory viruses like RSV. Cover preclinical studies, immunogenicity and safety testing, GLP/GCP compliance, and Phase I/II trial strategies. Develop expertise in ethics, regulatory filings, pharmacovigilance, data handling, and documentation for successful vaccine projects.

Elevify advantages

Develop skills

  • Design mRNA vaccines by planning constructs, LNPs, and GMP production.
  • Conduct immunogenicity assays like ELISA, neutralisation, ELISpot, and flow cytometry.
  • Plan preclinical studies selecting models, toxicity tests, and decision criteria.
  • Prepare regulatory files including IB, ethics, pharmacovigilance, and GCP compliance.
  • Co-design Phase I/II trials with endpoints, dosing, safety, and sampling 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.
Workload: between 4 and 360 hours

What our students say

I was just promoted to Intelligence Advisor for the Prison System, and the Elevify course 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
Great course. A lot of valuable information.
WiltonCivil Firefighter

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