It takes the average reader 2 hours and 13 minutes to read International Regulatory Harmonization Amid Globalization of Drug Development by Institute of Medicine
Assuming a reading speed of 250 words per minute. Learn more
The past several decades have been a time of rapid globalization in the development, manufacture, marketing, and distribution of medical products and technologies. Increasingly, research on the safety and effectiveness of new drugs is being conducted in countries with little experience in regulation of medical product development. Demand has been increasing for globally harmonized, science-based standards for the development and evaluation of the safety, quality, and efficacy of medical products. Consistency of such standards could improve the efficiency and clarity of the drug development and evaluation process and, ultimately, promote and enhance product quality and the public health. To explore the need and prospects for greater international regulatory harmonization for drug development, the IOM Forum on Drug Discovery, Development, and Translation hosted a workshop on February 13-14, 2013. Discussions at the workshop helped identify principles, potential approaches, and strategies to advance the development or evolution of more harmonized regulatory standards. This document summarizes the workshop.
International Regulatory Harmonization Amid Globalization of Drug Development by Institute of Medicine is 129 pages long, and a total of 33,411 words.
This makes it 44% the length of the average book. It also has 41% more words than the average book.
The average oral reading speed is 183 words per minute. This means it takes 3 hours and 2 minutes to read International Regulatory Harmonization Amid Globalization of Drug Development aloud.
International Regulatory Harmonization Amid Globalization of Drug Development is suitable for students ages 10 and up.
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