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The publication is an international standard on the design and operation of an efficient and accurate vital statistics system at national level. It provides guidelines on collection, compiling and disseminating vital statistics. More specifically it contains (a) basic principles for a vital statistics system; (b) uses of vital statistics and civil registration records; (c) topics to be covered in a vital statistics system; (d) sources of vital statistics and how they function; (e) quality assurance in the vital statistics system and (f) strategies in improving civil registration and vital statistics systems in countries. It also informs policy makers and the general public on the importance of vital statistics and hence further improving the vital statistics system.
This latest volume in the CQ Press series on vital statistics in American politics tackles interest groups and lobbying. This book builds from data that has been collected and organized from disclosure forms now required to be filed by registered lobbyists. After providing background about the Lobbying Disclosure Act, the book explores such questions as: When do organizations register to lobby? What are the characteristics of lobbying organizations (varying from professional and trade associations to businesses, coalitions, public interest groups, and intergovernmental groups)? How extensively do organizations lobby on issues? What sorts of efforts do they exert across Congress, the White House, and the various federal agencies? What is involved in terminations of lobbying firms and organizations? What sorts of issues and organizations are most often targeted? And what sorts of moneys are spent and how? Via narrative supported by extensive tables and charts, Vital Statistics on Interest Groups provides a broad, comprehensive, and informative view of lobbying, interest groups, and campaign contributions and their impact on American national politics.
Disparities in health and health care across racial, ethnic, and socioeconomic backgrounds in the United States are well documented. The reasons for these disparities are, however, not well understood. Current data available on race, ethnicity, SEP, and accumulation and language use are severely limited. The report examines data collection and reporting systems relating to the collection of data on race, ethnicity, and socioeconomic position and offers recommendations.
This book is a comprehensive text about all aspects of public health informatics and information technology. This books emphasizes the essential role that public health informatics plays in implementing a population-based health approach and to addressing chronic health conditions. This book is intended for public health specialists, nurses, medical informaticians, information technology professionals, and family physicians.