Vaccine Research and Development Course
Gain mastery in vaccine research from lab to human trials. Explore mRNA vaccine design, virology of RSV-like viruses, immunogenicity tests, GCP/GLP standards, and regulatory planning to develop safer, more effective vaccines in a contemporary lab environment. Ideal for building skills in compliant, high-quality vaccine programs.

flexible workload of 4 to 360h
valid certificate in your country
What will I learn?
This course offers a practical guide to creating and advancing mRNA vaccines for RSV-like respiratory viruses. You will cover preclinical study design, immunogenicity and safety testing, GLP/GCP compliance, and Phase I/II trial strategies. Build expertise in ethics, regulatory filings, pharmacovigilance, data handling, and team documentation for effective vaccine development.
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 documents including investigator brochures, ethics submissions, and GCP compliance.
- Collaborate on Phase I/II trials defining endpoints, dosing, 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 workloadWhat our students say
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