The Global Vaccine Safety Initiative (GVSI)

Background

In 2011, WHO and a group of partners developed a strategic document on vaccine safety called the Global Vaccine Safety Blueprint. This document sets out indicators that aim to ensure that all countries have at least a minimal capacity to ensure vaccine safety.

The Blueprint proposes a strategic plan for strengthening vaccine safety activities globally.
It focuses on building national capacity for vaccine safety in the world’s poorest countries through the coordinated efforts of major stakeholders.

The Blueprint was developed through a worldwide consultation of experts who defined its mission, vision and goals.

The Global Vaccine Safety Initiative, or GVSI, was set up to implement the Blueprint strategy. This comprises a framework of eight strategic objectives aimed at enhancing global vaccine safety activities. The strategic objectives focus on building and supporting a systemic approach to vaccine pharmacovigilance in all low- and middle-income countries.

Blueprint objectives 1–4 relate directly to the components of vaccine pharmacovigilance. Blueprint objectives 5–8 cover supporting elements that must be in place for the vaccine safety system to function effectively.

Reference documents

Report of the 7th Global Vaccine Safety Initiative (GVSI) meeting

The seventh meeting of the Global Vaccine Safety Initiative (GVSI) was held in Santiago, Chile from 8 to 9 October 2018, hosted by the Institute of Public...

Global vaccine safety blueprint - landscape analysis

Very few public-health interventions have been as successful as immunizations in preventing untimely deaths. Over the past thirty-five years, vaccines...

Global vaccine safety blueprint

Vaccines are administered in order to save lives and preserve health. They are among the safest medicinal products and are administered to healthy individuals, including...

Global Vaccine Safety Initiative implementation

The GVSI was set up to provide WHO and partners with a framework for enhancing vaccine pharmacovigilance.

Regulation and Prequalification
Progress towards enhancing regulatory practices related to medical products around the world is supported by capacity building, promoting regulatory convergence and harmonization.