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Modernization of Cosmetics Regulation Act

Client Alert | 1 min read | 08.16.23

In December 2022, the Modernization of Cosmetics Regulation Act (“MoCRA”)—the most significant expansion of the U.S. Food and Drug Administration's authority to regulate cosmetics in nearly 85 years—was signed into law. Among other things, MoCRA gives the FDA authority to require facility registration and reporting of serious adverse events, impose certain record-keeping obligations, recall cosmetic products, and establish good manufacturing practices. With many of MoCRA's provisions going into effect at the end of this year, cosmetics companies need to prepare to address these requirements and regulations, which may also have a considerable impact on the litigation landscape.

Crowell’s Product Risk Management team has written two publications to help cosmetics companies prepare for the big changes ahead.

See our Law360 article, “MoCRA Will Give Cosmetics Litigation A Makeover,” to learn more about the potential litigation impacts of MoCRA's requirements and steps companies can take now to manage their risk.

More extensive information on MoCRA can be found in our Modernization of Cosmetics Regulation Act White Paper. This white paper serves as a comprehensive overview of the history of cosmetics regulation in the United States, MoCRA’s new requirements and FDA’s new enforcement powers, potential litigation impacts, and specific action items companies can take now to best prepare themselves for MoCRA’s changes.

Insights

Client Alert | 2 min read | 04.21.25

Agencies to Curtail Unique, Customized Acquisitions in Favor of Commercial Products and Services

On April 16, 2025, the White House issued an Executive Order (“EO”), “Ensuring Commercial, Cost-Effective Solutions in Federal Contracts,” requiring agencies to meet their needs with commercially available products and services to the maximum extent practicable. The EO reiterates and builds upon the requirements set forth in the Federal Acquisition Streamlining Act of 1994 (“FASA”), which similarly encourages the use of commercial acquisition procedures. Specifically, the EO institutes a required review procedure for certain open acquisition actions and establishes an oversight procedure to be implemented for all acquisitions hereafter....