Kathleen Sanzo, J.D. is Co-Chair of Morgan Lewis' life sciences industry team. She centers her practice on regulatory and compliance issues connected to U.S. Food and Drug Administration (FDA)-regulated products. She leads and counsels clients on all legal and regulatory issues concerning food, dietary supplements, and cosmetic product manufacture, approval, marketing, and distribution; food, drug, and device compliance and enforcement matters; and consumer product issues regulated by the U.S. Consumer Product Safety Commission and state enforcement agencies, among other areas. A frequent author and co-author on publications related to FDA matters, Kathleen regularly speaks on these issues at industry events. She serves as Vice Chair of the Consumer Product Regulation Committee of the American Bar Association Section of Administrative Law and Regulatory Practice, and is a member of the Food and Drug Law Institute's Medical Products Committee.
In this episode of Food Safety Matters, we speak with Kathy [32:33] about:
News and Resources
News
FDA Releases Human Foods Program Priority Deliverables and Guidance Agenda for 2026 [5:48]
FDA Testing Pinpoints Contaminated Ingredient in Infant Botulism Outbreak [17:44]
EFSA Sets Safety Thresholds for Cereulide Toxin in Infant Formula [19:43]
EFSA to Advise on Cereulide Levels in Infant Formula Following Global Recall
UK Mother's Allegation that Recalled Nestlé Formula Sickened her Baby is Unconfirmed
Experts Share Lessons from a Successful Listeria 'Seek and Destroy' Process [23:36]
FDA to Hold Virtual Public Meeting on Food Allergen Thresholds, Releases Event Materials [29:44]
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