FDA Basics for the Drug and Medical Device Lawyer [DRI]

Denise Bense, a member of Cozen O’Connor’s Commercial Litigation Department, authored a section on “Medical Device Approvals” in DRI’s recently published “FDA Basics for the Drug and Medical Device Lawyer.” The book is designed to be a go-to reference guide for drug and device litigators, with straightforward explanations of the FDA’s regulation of the drug and medical device industry, including approval applications and processes, labeling, advertising and promotion, manufacturing, and post-approval commitments.

For more information, click here. To view the table of contents, click here

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Denise Brinker Bense



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