On December 18, 2023, the U.S Food and Drug Administration (FDA) provides guidance on submitting cosmetic product facility registrations and listings, outlining statutory requirements, definitions, submission responsibilities, submission informati
U.S. FDA
In response to persistent doubts being raised by consumer groups and scientists regarding the safety of cosmetics, as well as in the backdrop of implementation of the Modernization of Cosmetics Regulation Act of 2022 (MoCRA), which
The U.S.
FDA's Voluntary Cosmetic Registration Program (VCRP) is a reporting system for use by manufacturers, packers, and distributors of cosmetic products that are in commercial distribution in the United States.
The U.S. Food and Drug Administration (FDA) is announcing that it will move cosmetics regulation and color certification functions out of Center for Food Safety and Applied Nutrition (CFSAN) and into the Office of the Chief Scientist.
MoCRA defines federal cosmetics requirements for facility registration, safety evidence, good manufacturing practises, adverse event reporting, and more.
The MoCRA introduces new specifications for manufacturers and processors of cosmetics, gives the FDA additional enforcement power and mandates mandatory recalls, among other modifications.
California's Senator has appealed the lawmakers to include provisions related to safety reforms for personal care products in the U.S.