Erin Pannek

Hogan Lovells

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FDA and USDA Seek Feedback on Defining “Ultra-Processed Foods”

On July 24, 2025, the Food and Drug Administration (FDA) and U.S. Department of Agriculture (USDA) issued a joint request for information (RFI) to gather information and data to help the agencies develop a uniform definition...more

7/29/2025 / Food & Drug Regulations , Food Safety , Government Agencies , Proposed Rules , Public Health , Regulatory Requirements , State Legislatures , USDA

FDA issues letter to industry on recall communications for infant and baby foods

On July 9, 2025, the U.S. Food and Drug Administration (FDA) issued a letter from Commissioner for Human Foods Martin Makary and Deputy Commissioner for Human Foods Kyle Diamantas to industry members involved in the...more

7/17/2025 / Baby Products , Food and Drug Administration (FDA) , Food Safety , Product Recalls , Public Health , Regulatory Requirements , Reporting Requirements , Transparency

FDA Finalizes Guidance on Conducting Remote Regulatory Assessments

The Food and Drug Administration (FDA) published its final guidance for industry entitled “Conducting Remote Regulatory Assessments – Questions and Answers” on June 26, 2025. Initially published in draft format in July 2022...more

7/3/2025 / Food and Drug Administration (FDA) , Food Safety , Medical Devices , New Guidance , Regulatory Oversight , Regulatory Requirements

FDA announces expanded use of unannounced inspections at foreign manufacturing facilities

On May 6, 2025, the U.S. Food and Drug Administration (FDA) announced that it intends to expand its use of unannounced inspections at foreign manufacturing facilities. This announcement applies to facilities that produce...more

5/9/2025 / Food and Drug Administration (FDA) , Food Safety , Government Agencies , Imports , Manufacturers , New Regulations , Regulatory Oversight , Regulatory Requirements , Supply Chain

FDA issues Guidance on Interim Animal Food Ingredient Consultation (AFIC) Process

On January 6, 2025, the U.S. Food and Drug Administration’s (FDA) Center for Veterinary Medicine (CVM) issued its final guidance on the interim Animal Food Ingredient Consultation (AFIC) process, which FDA positions as a...more

1/9/2025 / Animal Food , Enforcement Actions , Final Rules , Food and Drug Administration (FDA) , Food Safety , Life Sciences , New Guidance , Regulatory Agenda , Regulatory Requirements , Veterinary Products

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