Tucker Ellis is pleased to announce that Mollie Benedict has co-edited DRI’s FDA Basics for the Drug and Medical Device Lawyer. Also contributing to the book are Tariq Naeem, Andrea Przybysz, and Brenda Sweet, co-authors of Chapter 2, “Drug Approvals, Medical Device Approvals, and Clinical Trials and Registries.” The “go-to” reference guide for drug and device litigators, the book provides straightforward explanations of the FDA’s regulation of the drug and device industry, including approval applications and processes, labeling, advertising and promotion, manufacturing, and post-approval commitments. For more information, click here.