Vaccine Research and Development Course
Gain expertise in vaccine development from laboratory design to early human trials. Master mRNA vaccine technology, virology of RSV-like viruses, immunogenicity testing, GLP/GCP standards, and regulatory strategies to create effective and safe vaccine candidates in contemporary lab environments. This course equips participants with practical knowledge for advancing innovative vaccine programs.

4 to 360 hours of flexible workload
certificate valid in your country
What Will I Learn?
This course provides a practical guide to developing mRNA vaccines for RSV-like respiratory viruses, covering preclinical study design, immunogenicity and safety testing, GLP/GCP compliance, and Phase I/II trial strategies. Participants will build expertise in ethics, regulatory filings, pharmacovigilance, data handling, and interdisciplinary documentation for robust vaccine initiatives.
Elevify Advantages
Develop Skills
- Design mRNA vaccines with construct planning, LNPs, and GMP production.
- Conduct immunogenicity assays including ELISA, neutralisation, ELISpot, and flow cytometry.
- Plan preclinical studies selecting models, toxicity evaluation, and decision criteria.
- Prepare regulatory submissions covering IB, ethics, pharmacovigilance, and GCP compliance.
- Collaborate on Phase I/II trial design with endpoints, dosing, 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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