Vaccine Research and Development Course
Gain expertise in vaccine development from lab to clinical trials. Master mRNA vaccine design for RSV-like viruses, virology basics, immunogenicity testing, GLP/GCP standards, and regulatory strategies to create effective, safe vaccines in contemporary labs. This course equips you with practical tools for compliant, high-impact vaccine programs spanning preclinical to early human studies.

4 to 360 hours flexible workload
valid certificate in your country
What will I learn?
This course provides a practical guide to developing mRNA vaccines for respiratory viruses like RSV. Key topics include preclinical study design, immunogenicity and safety testing, GLP/GCP compliance, and planning Phase I/II trials. Build expertise in ethics, regulatory filings, pharmacovigilance, data handling, and team documentation for robust 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 selecting models, toxicity tests, and decision criteria.
- Prepare regulatory dossiers covering IB, ethics, pharmacovigilance, 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 workload.What our students say
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