Vaccine Research and Development Course
Master vaccine research from lab bench to first-in-human trials. Learn mRNA vaccine design, RSV-like virology, immunogenicity assays, GCP/GLP compliance, and regulatory strategy to create safer, stronger vaccine candidates in a modern lab setup. This course builds practical skills for advancing respiratory virus vaccines through preclinical and early clinical stages.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
This course provides a practical guide to designing and developing mRNA vaccines for RSV-like respiratory viruses. You'll cover preclinical study design, immunogenicity and safety testing, GLP/GCP compliance, and planning for Phase I/II trials. Gain expertise in ethics, regulatory filings, pharmacovigilance, data handling, and team documentation for compliant vaccine programs.
Elevify advantages
Develop skills
- Design mRNA vaccines: plan constructs, LNPs, and GMP-ready production steps.
- Run vaccine immunogenicity assays: ELISA, neutralization, ELISpot, flow panels.
- Plan preclinical vaccine studies: choose models, define toxicity and go/no-go rules.
- Prepare vaccine regulatory files: IB, ethics/IRB, pharmacovigilance and GCP links.
- Co-design Phase I/II trials: endpoints, dose-escalation, safety and sampling.
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 are saying
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