This guideline deals with improving Civil Registration Systems and would supplement the UN manuals on the subject. Thus, this guideline is intended to assist national governments in general and CRVS organizations in particular for preparing national strategies and action plans for improving CRVS systems.

This course has been set up in response to the growing shortage of skilled population analysts in low and middle income countries, as identified by IUSSP and UNFPA, and the lack of post-graduate training in technical population analysis available to counteract this trend. The primary focus of this course is introducing the user to the methods used by demographers to analyse population data, and the sources of this data and the methods used to collect this data. Throughout the course, students are introduced to the types of issues of interest to demographers through real examples.

This handbook contains instructions for physicians on cause-of-death certification. It was prepared by the Department of Health and Human Services’ Centers for Disease Control and Prevention’s National Center for Health Statistics (NCHS). These instructions pertain to the 2003 revision of the U.S. Standard Certificate of Death and the 1992 revision of the Model StateVital Statistics Act and Regulations. This handbook serves as a model that can be adapted by any vital statistics registration area.

As part of the reporting structure of the Regional Action Framework on Civil Registration and Vital Statistics (CRVS) in Asia and the Pacific, by the end of 2015, members and associate members are required to submit a baseline report to the ESCAP Secretariat through their designated national focal point. The present document is intended to facilitate the compilation of national data and inputs for this baseline report.

This document provides guidance on identifying and mitigating risks associated with digital birth registration for implementing government agencies and their partners operating in low- and middle-income countries. It expands on the model of DBR developed by Plan International as part of its Count Every Child initiative and within the context of strengthening civil registration and vital statistics (CRVS) systems more broadly. The tool provides: checklists of likely risk factors, example risk mitigation mechanisms for each, and prompts to develop context-based responses.

This guide is intended to help build analytical capacity to assess the quality of mortality statistics that are currently being collected in order to improve their value in informing health policies and programs. To assist countries in validating and correcting their mortality data, the World Health Organization (WHO), in partnership with the Health Information Systems Knowledge Hub at the University of Queensland (UQ), Brisbane, has developed this mortality statistics assessment guide and toolkit.

This handbook contains instructions for medical examiners and coroners on the registration of deaths and the reporting of fetal deaths. It was prepared by the Department of Health and Human Services, Centers for Disease Control and Prevention, National Center for Health Statistics (NCHS). These instructions pertain to the 2003 revisions of the U.S. Standard Certificate of Death and the U.S. Standard Report of Fetal Death and the 1992 revision of the Model State Vital Statistics Act and Regulations.

The VAI was initially designed to be used by field reporters with minimal schooling and had only 18 symptom questions. It also allowed for the recording of a brief open-ended narrative, the place of death, any treatment by health services, and the type of treatment. The disease classification was based on Lay reporting of health information (WHO 1978) and COD was entered into the international form of the death certificate. Verbal autopsies (VAs) were physician-coded with reference to diagnostic algorithms.

This document highlights the importance of marriage and divorce registrations in Africa and presents the status of marriage and divorce registration, what is currently being done and recommendations for improvement.

Data2X, named for the power women have to multiply progress in their societies, aims to advance gender equality and women’s empowerment through improved data collection and analysis that can provide a solid evidence-base to guide development policy. To provide basic information for a Data2X roadmap, this report maps gender data gaps in developing countries across five domains of women’s empowerment: (1) health, (2) education, (3) economic opportunities, (4) political participation, and (5) human security.