Stakeholders' Understanding of European Medicine Agency's COVID-19 Vaccine Information Materials in EU and Regional Contexts
- PMID: 37897018
- PMCID: PMC10610863
- DOI: 10.3390/vaccines11101616
Stakeholders' Understanding of European Medicine Agency's COVID-19 Vaccine Information Materials in EU and Regional Contexts
Erratum in
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Correction: Castro et al. Stakeholders' Understanding of European Medicine Agency's COVID-19 Vaccine Information Materials in EU and Regional Contexts. Vaccines 2023, 11, 1616.Vaccines (Basel). 2025 Oct 13;13(10):1049. doi: 10.3390/vaccines13101049. Vaccines (Basel). 2025. PMID: 41150465 Free PMC article.
Abstract
The COVID-19 pandemic posed challenges to communicating accurate information about vaccines because of the spread of misinformation. The European Medicines Agency (EMA) tried to reassure the public by communicating early on about the development and approval of COVID-19 vaccines. The EMA surveyed patients/consumers, healthcare professional organizations, and individual stakeholders, both at the EU level and in an Italian regional context. The objectives of the study were to see if the EMA's core information materials were informative and well-understood and which communication channels were preferred by the public. The main findings showed that individual patients/consumers generally prefer to obtain information about COVID-19 vaccines from the internet or mass media, while organizations and individual healthcare professionals prefer to obtain information from national and international health authorities. Both at EU and local levels, participants had a good understanding of the key messages from regulators and found the materials useful and relevant. However, some improvements were recommended to the visual, text, and dissemination formats, including publishing more information on safety and using a more public-friendly language. Also, it was recommended to maintain the EMA's approach of using media, stakeholder engagement, and web-based formats to communicate about COVID-19 vaccines. In conclusion, user-testing of proactive communication materials aimed to prebunk misinformation during a public health crisis helps to ensure that users understand the development and safety of novel vaccine technologies. This information can then be used as a basis for further evidence-based communication activities by regulators and public health bodies in an emergency context.
Keywords: COVID-19; EMA; hesitancy; misinformation; vaccination.
Conflict of interest statement
I.C., R.G-Q., M.V.T., J.G.B., M.S. and N.B. have nothing to disclose. C.C. received throughout the University Hospital of Palermo (as an experimental center) funding grants for the conduction of clinical studies in the field of vaccination (RSV vaccination, high-dose influenza vaccination, PCV21 vaccination, study on co-administration of pediatric vaccination such as hexavalent, pneumococcal, and meningococcal B vaccines) and participated as a member to several national and international advisory boards on vaccines.
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References
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