Eric Greenberg has more than 30 years of experience representing clients in food and drug law matters, and he has been recognized worldwide for his capable handling of these often complex matters. Our firm’s dedicated focus on food and drug law puts us in a uniquely strong position to address your needs.
We regularly advise clients on regulatory compliance with requirements of the Food and Drug Administration (FDA) and state and local laws and represent them in actions related to alleged violations. We take the time to gain a complete understanding of our clients’ concerns and develop customized solutions designed specifically to address them.
Why Would FDA’s Emergency Actions Stick Around After the Emergency is Over?
By Eric F. Greenberg, Attorney-at-law
While some of the Food and Drug Administration’s actions in response to COVID-19 have been traditional, many others have been simplifications of regulatory requirements, and those simplifications could be made permanent.
Here’s one type of activity that was traditional: The agency has been slapping down phony drug products. The moment the COVID-19 pandemic hit the scene, dietary supplement products claiming to cure or prevent the virus started to be offered for sale, and immediately FDA and the Federal Trade Commission started making a regular habit of issuing stern warnings to the makers of the products.
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