One Hundred Years of Drug Regulation: Where Do We Go from Here?

Author:

Woosley Raymond L.1

Affiliation:

1. AZCERT Inc. and NDA Partners LLC, Oro Valley, Arizona 85755;

Abstract

The first 100 years of drug regulation by the US Food and Drug Administration (FDA) have been sculpted by a series of tragedies and the consequent broadening of the FDA's authority by Congress. The distinguishing feature of the FDA's execution of its mission is that it has routinely turned to science as the primary basis for decision making, and for this reason, it is one of the world's most respected regulatory agencies. Regulatory science, currently defined by the FDA as the science that underpins its decisions, has been the foundation for the FDA's success since its inception. This review focuses on the role of science as the basis for FDA decision making. It examines how regulatory science has made the FDA's past successes possible and concludes with an overview of how the FDA might augment its science-based regulation in the future and what new policy alternatives might be necessary.

Publisher

Annual Reviews

Subject

Pharmacology,Toxicology

Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Searching for COVID-19 treatments: First, do no harm;American Journal of Health-System Pharmacy;2020-08-03

2. FDA drug labeling: rich resources to facilitate precision medicine, drug safety, and regulatory science;Drug Discovery Today;2016-10

3. Attrition in Drug Discovery and Development;Attrition in the Pharmaceutical Industry;2015-10-30

4. Text and Data Mining Techniques in Adverse Drug Reaction Detection;ACM Computing Surveys;2015-07-21

5. Genomics in the land of regulatory science;Regulatory Toxicology and Pharmacology;2015-06

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