FDA in Flux
A Mintz newsletter tracking rapid changes in policy and agency actions that impact medical, life sciences, and consumer product investment decisions and development strategies.
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FDA in Flux — January 2026 Newsletter
January 22, 2026 | Article | By Joanne Hawana , Benjamin Zegarelli
The January 2026 edition of FDA in Flux highlights significant developments shaping the regulatory landscape for medical, life sciences, and consumer product sectors.
FDA in Flux — December 2025 Newsletter
December 16, 2025 | Article | By Joanne Hawana , Benjamin Zegarelli
The December 2025 edition of FDA in Flux highlights significant developments shaping the regulatory landscape for medical, life sciences, and consumer product sectors.
FDA in Flux — November 2025 Newsletter
November 19, 2025 | Article | By Joanne Hawana , Benjamin Zegarelli
The November 2025 edition of FDA in Flux highlights significant developments shaping the regulatory landscape for medical, life sciences, and consumer product sectors.
FDA in Flux – October 2025 Newsletter
October 16, 2025 | Article | By Joanne Hawana , Benjamin Zegarelli
The October 2025 edition of FDA in Flux highlights significant developments shaping the regulatory landscape for medical, life sciences, and consumer product sectors.
FDA in Flux — September 2025 Newsletter
September 17, 2025 | Article | By Joanne Hawana , Benjamin Zegarelli
The September 2025 edition of FDA in Flux highlights significant developments shaping the regulatory landscape for medical, life sciences, and consumer product sectors.
FDA in Flux — August 2025 Newsletter
August 14, 2025 | Article | By Joanne Hawana , Benjamin Zegarelli
The August 2025 edition of FDA in Flux highlights significant developments shaping the regulatory landscape for medical, life sciences, and consumer product sectors. Responding to President Trump’s executive order on reducing regulatory burdens, FDA announced the PreCheck program, with the goal of accelerating onshoring of drug manufacturing. FDA, HHS, and USDA have issued a joint request for data and information to develop a uniform definition of ultra-processed foods (UPF). FDA held a public meeting on August 4 to start negotiation for reauthorizing the Medical Device User Fee Amendments (MDUFA), providing a look at what stakeholders hope to achieve in terms of FDA commitments and performance goals. In July, FDA announced that it is revoking 52 individual “obsolete and unnecessary” food product standard-of-identity (SOI) regulations.
FDA in Flux — July 2025 Newsletter
July 9, 2025 | Article | By Joanne Hawana , Benjamin Zegarelli
The July 2025 edition of FDA in Flux highlights five significant developments shaping the regulatory landscape for medical, life sciences, and consumer product sectors.
FDA in Flux — June 2025 Newsletter
June 12, 2025 | Article | By Joanne Hawana , Benjamin Zegarelli
Welcome to FDA in Flux – A Mintz newsletter tracking rapid changes in policy and agency actions that impact medical, life sciences, and consumer product investment decisions and development strategies.
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