Vaccine Research and Development Course
Gain expertise in vaccine development from laboratory design to human trials. Master mRNA vaccine technology, virology of RSV-like viruses, immunogenicity testing, GLP/GCP standards, and regulatory strategies for creating effective, safe vaccines in contemporary labs. This course equips you with practical tools for advancing vaccine candidates through preclinical and early clinical stages.

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 RSV-like viruses, covering preclinical designs, immunogenicity and safety testing, GLP/GCP compliance, and Phase I/II trial strategies. Build expertise in ethics, regulatory filings, pharmacovigilance, data handling, and documentation for robust vaccine programmes.
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 investigator brochures, ethics, 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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