In 2022, the Modernization of Cosmetics Regulations Act of 2022 (MoCRA) was signed into law, bringing about the largest expansion of the U.S. Food and Drug Administration's (FDA) authority to regulate cosmetics since passage...more
1/27/2026
/ Cosmetics ,
Food and Drug Administration (FDA) ,
Information Reports ,
Modernization of Cosmetics Regulation Act of 2022 (MoCRA) ,
Personal Care Products ,
PFAS ,
Proposed Guidance ,
Public Health ,
Regulatory Agenda ,
Reporting Requirements ,
Risk Assessment ,
Scientific Research ,
Toxic Chemicals
Under the leadership of U.S. Food and Drug Administration (FDA) Commissioner Dr. Martin Makary, the agency has undergone significant change in the first year of President Donald Trump's second term. As part of the changes...more
1/8/2026
/ Animal Testing ,
Artificial Intelligence ,
Cannabis Products ,
Department of Health and Human Services (HHS) ,
Fee Agreements ,
Fees ,
Food and Drug Administration (FDA) ,
New Legislation ,
Over The Counter Drugs (OTC) ,
Pharmaceutical Industry ,
Proposed Rules ,
Public Comment ,
Regulatory Reform ,
Rulemaking Process ,
THC ,
Trump Administration
In accordance with President Donald Trump's Feb. 13, 2025, Executive Order (EO) 14212 to create a commission to Make America Healthy Again (MAHA), the Commission released its inaugural report, "The MAHA Report: Making Our...more
9/18/2025
/ Agribusiness ,
Chemicals ,
Department of Health and Human Services (HHS) ,
Executive Orders ,
Food and Drug Administration (FDA) ,
Food Labeling ,
Food Manufacturers ,
Food Safety ,
Information Reports ,
Pesticides ,
Public Health ,
Public Policy ,
Regulatory Reform ,
USDA
The Make America Healthy Again (MAHA) Commission was established by President Donald Trump's Feb. 13, 2025, executive order (EO) 14212 titled "Establishing the President's Make America Healthy Again Commission." As Holland &...more
9/15/2025
/ Centers for Medicare & Medicaid Services (CMS) ,
Comment Period ,
Department of Health and Human Services (HHS) ,
Environmental Protection Agency (EPA) ,
Executive Orders ,
Food and Drug Administration (FDA) ,
Health Care Providers ,
Healthcare ,
Information Reports ,
Life Sciences ,
National Institute of Health (NIH) ,
Pharmaceutical Industry ,
Public Health ,
Regulatory Oversight ,
Research and Development
The U.S. Food and Drug Administration (FDA) on Sept. 4, 2025, announced the release of 89 previously unpublished Complete Response Letters (CRLs), building on the previous release of more than 200 CRLs on July 10, 2025. The...more
States are rapidly enacting and implementing bans and reporting requirements for per- and polyfluoroalkyl substances (PFAS) in cosmetics, creating a complex and evolving compliance environment for manufacturers, distributors,...more
8/12/2025
/ Cosmetics ,
Distributors ,
Enforcement Actions ,
Hazardous Substances ,
Importers ,
Manufacturers ,
New Legislation ,
Personal Care Products ,
PFAS ,
Popular ,
Regulatory Requirements ,
Reporting Requirements ,
Retailers ,
State Attorneys General ,
State Bans ,
State Legislatures ,
Toxic Chemicals
Louisiana's Senate Bill 14 introduces a first-of-its-kind QR code labeling mandate for food products containing any of 44 specified ingredients, effective Jan. 1, 2028. The legislation follows Texas Senate Bill 25, which...more
7/29/2025
/ Business Strategies ,
Food and Drug Administration (FDA) ,
Food Labeling ,
Food Safety ,
New Legislation ,
Product Labels ,
Public Policy ,
Regulatory Requirements ,
Risk Management ,
Supply Chain ,
Toxic Chemicals ,
Toxic Substances Control Act (TSCA) ,
Warning Labels
The U.S. Food and Drug Administration (FDA) announced a final rule on July 16, 2025, revoking 52 standards of identity (SOIs) for food products that it deems obsolete. The FDA currently maintains more than 250 SOIs, and this...more
Over the first weeks of July 2025, the U.S. Food and Drug Administration (FDA) has issued several announcements heralding new policies and proposed regulatory changes that could dramatically impact the drug, biologics and...more
7/16/2025
/ Biologics ,
Consumer Protection Laws ,
Drug Pricing ,
Enforcement Actions ,
Expedited Approval Process ,
Expedited FDA Approval ,
Federal Food Drug and Cosmetic Act (FFDCA) ,
Food and Drug Administration (FDA) ,
Food Manufacturers ,
Pharmaceutical Industry ,
Prescription Drugs ,
Product Recalls ,
Proposed Regulation ,
Public Policy ,
Regulatory Agenda ,
Regulatory Reform
Texas Gov. Greg Abbott on June 22, 2025, signed Senate Bill 25 (SB 25), a law that, among other provisions, requires the following consumer warning labeling on foods containing any of 44 ingredients: "WARNING: This product...more
7/2/2025
/ Chemicals ,
Food and Drug Administration (FDA) ,
Food Labeling ,
Food Manufacturers ,
Food Safety ,
Governor Abbott ,
New Legislation ,
Preemption ,
Regulatory Requirements ,
Rulemaking Process ,
State and Local Government ,
Warning Labels
The U.S. Food and Drug Administration (FDA) is overhauling its approach to post-market oversight of food chemicals, marked by the proposed rollout of a new Post-Market Assessment Prioritization Tool. The FDA first announced...more
7/1/2025
/ Chemicals ,
Food and Drug Administration (FDA) ,
Food Manufacturers ,
Food Safety ,
GRAS ,
Proposed Rules ,
Public Health ,
REACH ,
Regulatory Oversight ,
Regulatory Reform ,
Risk Assessment ,
Rulemaking Process ,
Toxic Chemicals ,
Toxic Substances Control Act (TSCA)
The Make America Healthy Again (MAHA) Commission, as established by President Donald Trump's Feb. 13, 2025, Executive Order (EO) 14212, released its inaugural report on May 22, 2025, titled "The MAHA Report: Making Our...more
5/27/2025
/ Artificial Intelligence ,
Chemicals ,
Clinical Trials ,
Environmental Protection Agency (EPA) ,
Food and Drug Administration (FDA) ,
Food Manufacturers ,
Food Supply ,
Information Reports ,
Pesticides ,
Prescription Drugs ,
Public Health ,
Regulatory Reform ,
Toxic Chemicals ,
Trump Administration
The U.S. Food and Drug Administration (FDA) has announced a new initiative to systematically review the safety of chemicals already in the nation's food supply....more
5/23/2025
/ Chemicals ,
EU ,
Federal Food Drug and Cosmetic Act (FFDCA) ,
FIFRA ,
Food & Drug Regulations ,
Food and Drug Administration (FDA) ,
Food Manufacturers ,
Food Safety ,
Proposed Rules ,
Proposition 65 ,
Public Comment ,
Regulatory Oversight ,
Regulatory Reform ,
Toxic Chemicals ,
Toxic Substances Control Act (TSCA)
The U.S. Department of Health and Human Services (HHS) and U.S. Food and Drug Administration (FDA) on April 22, 2025, announced their intent to phase out the use of certain food additives, including petrochemical-based dyes,...more
In this episode of Holland & Knight's "The Eyes on Washington" podcast series, attorneys Rachel Gartner, Sara Klock, John Vaughan and Michael Werner discuss the evolving landscape of U.S. Food and Drug Administration (FDA)...more
In recent months, in response to increased consumer interest, federal and state government officials have taken action to propose and adopt laws and regulations directed at promoting consumer transparency and encouraging...more
4/3/2025
/ Disclosure Requirements ,
Environmental Policies ,
Fashion Industry ,
Greenhouse Gas Emissions ,
Manufacturers ,
New Legislation ,
PFAS ,
Proposed Legislation ,
Regulatory Requirements ,
Sustainability ,
Textiles
U.S. Department of Health and Human Services (HHS) Secretary Robert F. Kennedy Jr. announced on March 10, 2025, that he directed the acting commissioner of the U.S. Food and Drug Administration (FDA) to explore potential...more
The U.S. Food and Drug Administration (FDA) is taking a stronger approach toward supporting health goals in 2025 and beyond by setting the tone and releasing a number of regulatory actions aimed at enhancing consumer health...more