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 develop safer, stronger vaccine candidates in a modern laboratory setting. This course provides practical guidance on preclinical studies, trial planning, ethics, data management, and cross-functional documentation for compliant vaccine programs.

from 4 to 360h flexible workload
certificate valid in your country
What will I learn?
This course offers a practical roadmap for designing and advancing mRNA vaccines against RSV-like respiratory viruses. Key topics include preclinical study design, immunogenicity and safety assays, GLP/GCP compliance, Phase I/II trial planning, ethics, regulatory submissions, pharmacovigilance, data management, and documentation for high-quality vaccine development.
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 say
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Course in PDF