Vaccine Research and Development Course
Gain expertise in vaccine research from lab to human trials. Master mRNA vaccine design for RSV-like viruses, virology basics, immunogenicity testing, GCP/GLP standards, and regulatory strategies to create safer, more effective vaccines in contemporary labs. This course builds practical skills for compliant, high-quality vaccine development across preclinical and early clinical stages.

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