A Dedicated Focus On Food And Drug Law And Business Litigation Matters

If you are in an industry that in any way involves food, dietary supplements, over-the-counter drugs, medical devices, cosmetics or the packaging that contains them, it is important that you have dedicated counsel from a firm that knows the law and has the ability to help you ensure compliance. For more than 30 years, attorney Eric Greenberg and his team at Eric F. Greenberg, P.C., have been protecting clients’ business interests through strategic planning and skillful representation.

Our dedicated focus on food and drug law and packaging law allows us to provide innovative and comprehensive compliance solutions. A large portion of our practice is dedicated to advising clients on compliance requirements and the steps that need to be taken in order to remain compliant with Food and Drug Administration (FDA) regulations. Over the years, we have also developed a robust business litigation practice that includes services for contract disputes and the protection of trade secrets.

Our clients appreciate the personalized service they receive from our attorneys. We work closely with corporate officers and other key personnel in order to fully understand your business needs and deliver the most timely and relevant service possible.

To learn more about our Chicago, Illinois-based lawyers and other personnel, please select a link from the list below.

Principal Attorney

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Contact Us To Discuss Your Legal Needs

We invite you to schedule an initial consultation to learn more about our law firm’s food and drug law services. You can reach us by phone at 312-977-4647 or via email for an initial consultation.

Our firm is a proud member of the International Network of Boutique Law Firms, a select organization with member law firms throughout the United States and “strategic partners” around the world.


INBFL INTERNATIONAL NETWORK OF BOUTIQUE & INDEPENDENT LAW FIRMS
Food Section

Why Would FDA’s Emergency Actions Stick Around After the Emergency is Over?

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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Phone: 312-977-4647