Medical Library Amendments of 1969
Author | : United States. Congress. Senate. Committee on Labor and Public Welfare. Subcommittee on Health |
Publisher | : |
Total Pages | : 252 |
Release | : 1969 |
Genre | : Federal aid to medical libraries |
ISBN | : |
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Author | : United States. Congress. Senate. Committee on Labor and Public Welfare. Subcommittee on Health |
Publisher | : |
Total Pages | : 252 |
Release | : 1969 |
Genre | : Federal aid to medical libraries |
ISBN | : |
Author | : United States. Congress. Senate. Committee on Labor and Public Welfare. Subcommittee on Health |
Publisher | : |
Total Pages | : 252 |
Release | : 1969 |
Genre | : Federal aid to medical libraries |
ISBN | : |
Considers S. 2239 and related S. 2549 and H.R. 11702, to extend the Medical Library Assistance Act of 1965. Includes letters supporting extension of the Act from members of the Medical Library Association organized by state (p. 77-205).
Author | : National Library of Medicine (U.S.) |
Publisher | : |
Total Pages | : 1088 |
Release | : 1965 |
Genre | : Medicine |
ISBN | : |
Author | : National Library of Medicine (U.S.) |
Publisher | : |
Total Pages | : |
Release | : 1970 |
Genre | : Medicine |
ISBN | : |
First multi-year cumulation covers six years: 1965-70.
Author | : United States. Congress |
Publisher | : |
Total Pages | : 1324 |
Release | : 1968 |
Genre | : Law |
ISBN | : |
Author | : United States. Department of the Interior. Library |
Publisher | : |
Total Pages | : 732 |
Release | : 1969 |
Genre | : Library catalogs |
ISBN | : |
Author | : United States. Congress. Senate. Committee on Labor and Public Welfare |
Publisher | : |
Total Pages | : 2032 |
Release | : 1971 |
Genre | : Labor policy |
ISBN | : |
Author | : Institute of Medicine |
Publisher | : National Academies Press |
Total Pages | : 141 |
Release | : 2010-10-04 |
Genre | : Medical |
ISBN | : 0309162904 |
The Food and Drug Administration (FDA) is responsible for assuring that medical devices are safe and effective before they go on the market. As part of its assessment of FDA's premarket clearance process for medical devices, the IOM held a workshop June 14-15 to discuss how to best balance patient safety and technological innovation. This document summarizes the workshop.
Author | : World Health Organization |
Publisher | : World Health Organization |
Total Pages | : 82 |
Release | : 2008-12-15 |
Genre | : Medical |
ISBN | : 9241580410 |
In response to the call of the 48th World Health Assembly for a substantial revision of the International Health Regulations, this new edition of the Regulations will enter into force on June 15, 2007. The purpose and scope of the Regulations are "to prevent, protect against, control and provide a public health response to the international spread of disease in ways that are commensurate with and restricted to public health risks, and which avoid unnecessary interference with international traffic and trade." The Regulations also cover certificates applicable to international travel and transport, and requirements for international ports, airports and ground crossings.