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Many ANSI regulations are incorporated by reference into United States federal statutes (i.e. by OSHA regulations referring to individual ANSI specifications). ANSI does not make these standards publicly available, and charges money for access to these documents; it further claims that it is copyright infringement for them to be provided to the ...
During the debate in Congress, more than one version of the clause was considered. Here is the first version: "The Congress shall have power to make all laws which shall be necessary and proper to secure ... to all persons in the several states equal protection in the rights of life, liberty, and property."
In print, Raymond Briggs' graphic novel When the Wind Blows (later adapted as an animated film, radio and stage play) obliquely mentions various aspects of the Protect and Survive programme. The leaflet series became the subject of detailed and scholarly criticism from anti-nuclear authors (such as E. P. Thompson ), who produced a ...
The Articles of Confederation, ratified by the colonies in 1781, provided: . The United States in Congress assembled shall also have the sole and exclusive right and power of regulating the alloy and value of coin struck by their own authority, or by that of the respective states—fixing the standards of weights and measures throughout the United States.
An English version released in 2006 contained about 2,000 articles. [ W 103 ] The Polish-language version from 2006 contains nearly 240,000 articles, [ W 104 ] the German-language version from 2007/2008 contains over 620,000 articles, [ W 105 ] and the Spanish-language version from 2011 contains 886,000 articles.
Under Title III of the ADA, all new construction (construction, modification or alterations) after the effective date of the ADA (approximately July 1992) must be fully compliant with the Americans With Disabilities Act Accessibility Guidelines (ADAAG) [13] found in the Code of Federal Regulations at 28 C.F.R., Part 36, Appendix A.
ISO 13485 Medical devices -- Quality management systems -- Requirements for regulatory purposes is a voluntary standard, [1] published by International Organization for Standardization (ISO) for the first time in 1996, and contains a comprehensive quality management system for the design and manufacture of medical devices.