Experienced Merger And Acquisition Attorneys

Mergers and acquisitions are extremely complex business transactions that require careful analysis and execution at every stage. There can be regulatory issues that need to be considered in many cases, particularly in transactions involving companies in FDA-regulated industries.

Providing FDA Regulatory Compliance And Due Diligence Support

The lawyers at the law firm of Eric F. Greenberg, P.C., provide experienced representation in mergers and acquisitions and related issues. Our extensive experience in the areas of food and drug law and packaging law allows us to provide invaluable insight into the unique issues that need to be considered in these matters.

A timely and thorough assessment of FDA compliance risk can help you avoid a bad deal, reflect risk in your pricing decisions or just help you gain an early understanding of what is needed to keep compliant in the FDA environment. From pre-audit reviews of your compliance program to support in any aspect of the due diligence process, we are prepared to provide the attentive service you require.

Contact Our Office To Discuss Your Needs With An Attorney

Contact our Chicago, Illinois, office to learn more about our mergers and acquisitions and due diligence support services. You can reach us by phone at 312-977-4647 or contact us via email.

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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