Published in Medical Letter on the CDC and FDA, October 19th, 2003
"The process of clinical development and regulatory review of new therapeutics in the United States was significantly changed by a number of legislative acts passed in the 1980s and 1990s. These acts were designed to encourage the development of innovative products, especially for rare, serious or life-threatening diseases, and to ensure that patients had timely access to these treatments," a scientist in the United States reports.
"To assess the effects of the various...
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