Case Studies Best of the United States 2017

IPS

Under the best of conditions, a painstakingly long and expensive process—on average, 10 years and $2.6 billion—awaits any prescription drug seeking to achieve regulatory approval. There are the research and discovery phases, the preclinical testing, the initial application to the Food and Drug Administration, several rounds of clinical testing, final new drug application and follow-up […]

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Spring 2018

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