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 compliance, and regulatory strategies to create effective, safe vaccines in modern labs. This course provides practical tools for preclinical studies, trial planning, ethics, data handling, and compliant programs.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
This course offers a practical guide to mRNA vaccine design and development for respiratory viruses like RSV. Key topics include preclinical study design, immunogenicity and safety testing, GLP/GCP compliance, Phase I/II trial strategies, ethics, regulatory filings, pharmacovigilance, data management, and team documentation for successful vaccine programs.
Elevify advantages
Develop skills
- Design mRNA vaccines by planning constructs, LNPs, and GMP production.
- Conduct immunogenicity assays including ELISA, neutralization, ELISpot, and flow cytometry.
- Plan preclinical studies selecting models, toxicity tests, and decision criteria.
- Prepare regulatory submissions covering IB, ethics, pharmacovigilance, and GCP.
- Co-design Phase I/II trials with endpoints, dosing, safety, and sampling plans.
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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