This project is part of an initiative that will provide evidence and strengthen capacity for bridging the knowledge gap in responding to the growing COVID-19 health crisis both in the short term and in the longer term.
The Global Partnership for Education (GPE) and IDRC launched the Knowledge and Innovation Exchange (KIX) to improve policies and practices that will strengthen national education systems within GPE partner countries.
Digital health technologies have the potential to provide greater access to better quality and more affordable care, but governing the digital personal data generated by and required to support many digital health innovations is a critical challenge.
There is a significant gap in data concerning the patterns and drivers of transactional sex, sexual exploitation, and abuse in transactional sex and their implications on the sexual and reproductive health and rights of refugees.
This project will promote research evidence and data-informed decision-making and accelerate achievement of the Sustainable Development Goals (SDGs) in two selected countries in the Middle East namely Lebanon and Jordan.
The research will promote greater disaggregation of health information and inclusion of gender and social determinants of health indicators in Health Information Systems (HIS) at the national level in Egypt, Jordan and Morocco.
In an era of rapid change and increasing mistrust in institutions, open data and the surrounding communities that use it, are working to shift norms and culture to create dialogue and collaboration between governments, civil society and the private sector.
The current global refugee system is failing refugees and the states that host them, despite the often-heroic efforts of sympathetic states, international organizations, civil society, and refugees themselves.
This project aims to generate knowledge on adolescents’ perceptions of and requirements for sexual and reproductive health (SRH) services among Palestinian refugee camp dwellers in the West Bank and Jordan.
The lack of reliable data limits the ability of health providers, planners, and community members to make informed decisions that can influence the well-being of women and children, particularly in vulnerable and undercounted populations.