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    VAC4EU
    • Is a not-for profit international association, with institutional memberships (study network)
    • Provides access to a well characterised public study network, which can provide data access and perform studies for different internal and external requesters such as vaccine manufacturers, European Commission, regulators, public health institutes.
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Pfizer ABRYSVO® Post-Authorisation Safety Study – Hepatically and renally impaired

The purpose of this study is to assess the safety profile of the Pfizer RSV vaccine in renally and hepatically impaired older adults.

Pfizer/BioNTech Comirnaty® Post-Authorisation Safety Study

The primary aim of this study was to determine whether there is an increased risk of AESI after receiving the Pfizezr/BioNTech COVID-19 vaccine.

Pfizer/BioNTech Comirnaty® myocarditis and pericarditis study

The aim of this study is to characterise the clinical course of myocarditis and/or pericarditis diagnosed after receiving the Pfizer-BioNTech COVID-19 vaccine

Pfizer/BioNTech Comirnaty® bivalent Post-Authorisation Safety Study

The aim of this study is to assess whether there is an increased risk of AESI after receiving the bivalent Pfizer/BioNTech COVID-19 vaccine.

Moderna Spikevax® myocarditis and pericarditis study

The primary objective of this study is to identify risk factors for myocarditis and pericarditis after vaccination with the Moderna COVID-19 vaccine, as well as to characterise the clinical course […]

Moderna Spikevax® Post-Authorisation Safety Study

The primary objective of this study is to assess whether vaccination with the Moderna COVID-19 vaccine is associated with increased rates of AESI in the general population, with a secondary […]

Moderna Spikevax® Post-Authorisation Safety Study – Pregnancy

The primary objective of this study is to assess whether there is a higher risk of pregnancy and/or neonatal complications or adverse outcomes after exposure to the Moderna COVID-19 vaccine, […]

Janssen Jcovden® Post-Authorisation Safety Study

The first aim of the study was to conduct a feasibility assessment on a safety evaluation study on the Janssen COVID-19 vaccine, then to assess the risk of developing AESI […]

AstraZeneca AZD1222 Post-Authorisation Safety Study

This study aimed to evaluate the incidence and relative risk of AESI after receiving the AstraZeneca COVID-19 vaccine.

(Early) COVID-19 Vaccine Monitor – cohort event monitoring via primary and secondary data collection

This study aimed to monitor AESI prior and following COVID-19 vaccination, in order to estimate incidence rates and pick up signals.

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VAC4EU (Vaccine monitoring Collaboration for Europe) is the sustainability solution of the ADVANCE project which was funded by the Innovative Medicines Initiative from October 2013 - March 2019.

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