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Description:The data collection program of the National Center for Health Statistics during the 1980's is described in this report. The systems are grouped by the origin of the data --the vital statistics registration system, provider-based surveys, and population-based surveys. This document is designed to provide a brief description of each of the data collection systems, some of the most important information derived from the system, references for readers who want more detailed descriptions, and the means of releasing information through publications and public-use data files.
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Content Notes:Includes bibliographical references.
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Pubmed ID:7324381
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Pages in Document:print; v, 21 p. ; 28 cm.
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