In 2014, at the Sixty-seventh World Health Assembly, 194 Member States endorsed the Every Newborn: an action plan to end preventable deaths (Resolution WHA67.10), a road map of strategic actions to end preventable newborn mortality and stillbirths and contribute to reducing maternal mortality and morbidity. The Every Newborn Action Plan presents evidence-based solutions and sets out a clear path to 2020 with eight specific milestones for what needs to be done differently to greatly reduce mortality rates and improve maternal and newborn health by 2030.
Plan International Australia proposes developing a standards-based software solution to provide for civil registration and population data needs in low resource settings. The open source CRVS platform will be free, fully compliant, and adaptable for different country contexts in Asia and the Pacific. The software will be easy to deploy, user-centric, and require minimal skills for customisation, maintenance and support.
As healthcare challenges continue to mount worldwide, effective data use and sharing is imperative. In support of health information sharing as a public good, WHO and it’s Director-General’s office is working to finalize a Policy on Use and Sharing of Data Collected in Member States by the WHO Outside the Context of Public Health Emergencies. The document sets out a systematic and comprehensive approach to data use and data sharing.
WHO, in collaboration with Canada, UNICEF, USAID and the World Bank, organized a technical meeting in Geneva from 17 to 18 December 2013 to share experiences and explore the potential of health sector innovation for strengthening CRVS systems. This paper describes key areas in which health innovations can contribute to CRVS systems strengthening and lays out good practices against which health sector activities should be assessed.
This document has been developed through a consultative process involving country representatives from the health, civil registration and statistics sectors, technical experts, researchers, and representatives of agencies, donors and development partners. As part of this process, a technical meeting, Improving Mortality Statistics as part of Strengthening Civil Registration and Vital Statistics Systems, World Health Organization, Technical Meeting, was convened by WHO from 4 to 5 November 2014 in Geneva, Switzerland.
The note outlines the content and key issues addressed during the 2014 Ministerial Conference special sessions.
This material was presented at the Ministerial Conference on Civil Registration and Vital Statistics 24 – 28 November 2014, by Ms. Kendra Gregson, Senior Advisor, Social Welfare and Justice Systems, UNICEF
This material was presented at the Ministerial Conference on Civil Registration and Vital Statistics 24 – 28 November 2014, by Mr. Mark Landry, Coordinator, Health Intelligence and Innovation Division of Health Systems, WHO Regional Office for the Western Pacific
This material was presented at the Ministerial Conference on CRVS by Mr. Edward Duffus, Digital Birth Registration Manager, Plan International.
A review of the quality of cause of death data from 115 WHO member countries, published in 2005, categorized South Africa as having low quality cause of death data based on a combination of a more than 20% of deaths being ill-defined deaths and less than 70% of deaths being registered.
In recent years, the Government of Pakistan has demonstrated increased commitment to social sector development, consequently leading to some notable successes. In particular, the country is celebrating the recent achievement of the Millennium Development Goal (MDG) for sanitation, halving the proportion of the population without sustainable access to basic sanitation. Over the past two decades, the government has also made notable strides in combatting polio, increasing routine immunization and decreasing the number of out-ofschool children.
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