Vaccine Research and Development Course
Gain expertise in vaccine research from laboratory design to first-in-human trials. Master mRNA vaccine development, virology of RSV-like viruses, immunogenicity testing, GCP/GLP standards, and regulatory strategies to create safer and more effective vaccine candidates in contemporary lab environments. This course equips you with practical skills for compliant vaccine programs.

flexible workload of 4 to 360h
valid certificate in your country
What will I learn?
This course offers a practical guide to designing and developing mRNA vaccines for RSV-like respiratory viruses. Key topics include preclinical study design, immunogenicity and safety testing, GLP/GCP compliance, and planning for Phase I/II trials. Develop proficiency in ethics, regulatory filings, pharmacovigilance, data handling, and documentation for high-quality vaccine initiatives.
Elevify advantages
Develop skills
- Design mRNA vaccines by planning constructs, LNPs, and GMP production steps.
- Conduct immunogenicity assays including ELISA, neutralisation, ELISpot, and flow cytometry.
- Plan preclinical studies selecting models, toxicity assessment, and go/no-go criteria.
- Prepare regulatory submissions covering IB, ethics/IRB, pharmacovigilance, and GCP compliance.
- Collaborate on Phase I/II trial design with endpoints, dose escalation, safety, and sampling plans.
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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