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U.S. Innovation and Competition Act; Long title: To establish a new Directorate for Technology and Innovation in the National Science Foundation, to establish a regional technology hub program, to require a strategy and report on economic security, science, research, innovation, manufacturing, and job creation, to establish a critical supply chain resiliency program, and for other purposes.
Authorizes an all-of-government approach to promoting competition and creates a White House Competition Council. Executive Order 14036 , titled Executive Order on Promoting Competition in the American Economy and sometimes referred to as the Executive Order on Competition , [ 1 ] is the fifty-first executive order signed by U.S. President Joe ...
The legislation would inject competition into the credit card market to lower costs. For the majority of New Jersey businesses, this change cannot come soon enough. More perspective: A crisis?
The Unlocking Consumer Choice and Wireless Competition Act was introduced into the United States Senate on March 11, 2013 by Sen. Patrick J. Leahy (D, VT). [8] It was referred to the United States Senate Committee on the Judiciary. On July 15, 2014, the Senate voted to pass the bill with unanimous consent. [8]
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The America COMPETES Act (formally America Creating Opportunities to Meaningfully Promote Excellence in Technology, Education, and Science Act of 2007) [1] [2] [3] was authored by Bart Gordon [4] and signed into law on August 9, 2007, by President George W. Bush. The act aimed to invest in innovation through research and development and improve ...
Local NAACP branches would be called upon to sponsor ACT-SO, conduct local competitions annually, and then take local gold medalists to an annual national ACT-SO competition. 1978: The first National ACT-SO competition was held in Portland, Oregon with seven cities participating: Atlanta, Baltimore, Chicago, Kansas City, Los Angeles, New ...
The Act's two main goals are to facilitate entry of generic drugs into the market and to compensate the original drug developers for regulatory delays by the Food and Drug Administration. It is generally believed that the Act accomplished both goals: encouraging development of new medications and accelerating market entry of generics. [1]