Vaccine Research and Development Course
Gain mastery in vaccine research from laboratory experiments to initial human trials. Explore mRNA vaccine creation, virology of RSV-like viruses, immunogenicity tests, GCP/GLP standards, and regulatory approaches to develop safer and more potent vaccine options in a contemporary lab environment. This training equips participants with essential knowledge for advancing vaccine innovation while ensuring compliance and safety throughout the development process.

flexible workload from 4 to 360h
valid certificate in your country
What will I learn?
This course offers a clear, hands-on guide to creating and improving mRNA vaccines for RSV-type respiratory viruses. You will cover preclinical study planning, immunogenicity and safety testing, GLP/GCP connections, and Phase I/II trial preparation. Build expertise in ethics, regulatory filings, pharmacovigilance, data handling, and team documentation for effective, compliant 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 by selecting models, toxicity assessment, and decision criteria.
- Prepare regulatory documents covering IB, ethics, pharmacovigilance, and GCP compliance.
- Collaborate on Phase I/II trials with focus on endpoints, dosing, safety, and sampling.
Suggested summary
Before starting, you can change the chapters and 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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