National Law Review
7/23/2026
![FDA’s 2026 Enforcement Priorities: What In-House Counsel Must Know [Video]](https://natlawreview.com/sites/default/files/styles/article_image/public/2026-07/FDA_food_drug_adm_web_SMALL.jpg.webp?itok=_6oi-TEI)
FDA’s 2026 Enforcement Priorities: What In-House Counsel Must Know [Video]
Short summary
The FDA's 2026 enforcement priorities span six key trends including monitoring online marketing claims, cracking down on telehealth platforms offering compounded GLP-1s, enforcing CGMP compliance, and scrutinizing food facility Foreign Supplier Verification Programs. Form 483 responses are under heightened scrutiny, and medical device manufacturers should prepare for increased QMSR enforcement. In-house counsel should watch for shifts under new FDA leadership.
- •FDA monitoring websites, social media, and podcasts for inappropriate marketing claims
- •Continued enforcement against telehealth platforms offering compounded GLP-1s
- •Form 483 responses under heightened scrutiny; device makers should prepare for QMSR enforcement
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