- Posts by Caitlin Carlton
AssociateAttorney Caitlin Carlton supports health care and life sciences organizations in a wide range of legal and regulatory matters.
With a detail-oriented, client-focused approach, Caitlin advises clients on compliance with health ...
Blogs
6 minute read
Legislation introduced in the U.S. Senate in November, informally called the “Better FDA Act of 2025,” is perhaps a bit misleading. While it involves the Food and Drug Administration (“FDA”), the full title of S. 3122—introduced on November 6—is actually “The Better Food Disclosure Act of 2025,” designed to amend the federal Food, Drug, and Cosmetic Act (“FDCA”) regarding food substances generally recognized as safe (“GRAS”).
Blog Editors
Recent Updates
- IRS Issues Guidance Regarding Group Exemption Letters
- Legislative Push for FDA Preemptive Authority Over Dietary Supplement Regulation
- GUARD and GLOBE Pricing Models Could Test Manufacturer Rebates for Medicare Part B and D Drugs
- FDA’s Office of Dietary Supplement Programs Signals Key Enforcement and Policy Priorities for the Year Ahead
- OIG Issues Guidance, Request for Information on DTC Programs