ARTICLE
2 February 2021

2020 Enforcement Review: FDA-Regulated Medical Products And Food Safety

RG
Ropes & Gray LLP

Contributor

Ropes & Gray is a preeminent global law firm with approximately 1,400 lawyers and legal professionals serving clients in major centers of business, finance, technology and government. The firm has offices in New York, Washington, D.C., Boston, Chicago, San Francisco, Silicon Valley, London, Hong Kong, Shanghai, Tokyo and Seoul.
The dynamic nature of the COVID-19 pandemic demanded an all-hands-on-deck approach to enforcement in 2020 by the U.S. Food and Drug Administration ("FDA"),
United States Food, Drugs, Healthcare, Life Sciences

 The dynamic nature of the COVID-19 pandemic demanded an all-hands-on-deck approach to enforcement in 2020 by the U.S. Food and Drug Administration ("FDA"), the Department of Justice ("DOJ"), and other regulatory and law enforcement agencies. Protecting the public from those who sought to exploit opportunities to make a quick buck by marketing quack COVID-19 cures, unproven COVID-19 prevention products and substandard personal protective equipment quickly emerged as top government enforcement priorities. This review revisits the year's key FDA and DOJ enforcement actions related to FDA-regulated products, and offers insights into likely enforcement priorities for 2021.

The content of this article is intended to provide a general guide to the subject matter. Specialist advice should be sought about your specific circumstances.

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