CIRS will attend In-cosmetics Global 2026 in Paris, providing cosmetic regulatory compliance, market access, and efficacy testing services at Stand 2D59.

From March 18 to 20, 2026, the three-day PCHi exhibition came to a successful close at the Hangzhou International Convention and Exhibition Center. As a key event in the global cosmetics, personal care, and home care industries, this year’s show brought together numerous leading domestic and international enterprises and industry elites.

Health Canada is implementing new regulations that will require cosmetic manufacturers to disclose specific fragrance allergens directly on product labels, marking a shift from current practices that allow fragrance ingredients to be listed collectively under "parfum" or "fragrance."

CIRS is delighted to announce that we will be exhibiting at the PCHi in Hangzhou, China between 18-20 March, 2026.

Food contact plastics entering the European market are regulated by EU regulation EU 10/2011. EU legislation is based on the "positive list" principle, where substances used to manufacture food contact plastic materials must be selected from the list in Annex I of EU regulation EU 10/2011. Only substances listed can be added as monomers, additives, or production aids in the manufacturing formula. In the actual production process, apart from substances intentionally added during the process, there are also Non-Intentionally Added Substances (NIAS).

On January 29, 2026, the European Commission published Directive (EU) 2026/192, amending the Toy Safety Directive 2009/48/EC to permit the use of cobalt in three specific applications within toys.

On February 4, 2026, ECHA announced the official inclusion of n-Hexane and 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]diphenol (BPAF) and its salts into the SVHC candidate list.

On February 2, 2026, the Taiwan Food and Drug Administration (TFDA), under the Ministry of Health and Welfare, announced a revision to the annex of the Documentation Required for Case-by-Case Review of Applications for the Use of Human Cell-Derived Exosomes in Cosmetics. The revised annex takes effect immediately upon the date of announcement.

The Labeling of Hazardous Art Materials Act (LHAMA) requires all art materials to be evaluated for chronic health hazards. Materials posing such risks must have appropriate warning labels. This law applies to all art materials, not just those for children. Under U.S. Consumer Product Safety Commission (CPSC) regulations (16 CFR §1500.14(b)(8)), art materials must undergo LHAMA assessment and labeling in accordance with ASTM D4236.

On January 15, 2025, China’s National Institutes for Food and Drug Control (NIFDC) issued a notice announcing the release of three draft cosmetic standards aimed at further enhancing the country’s technical framework for cosmetics. The drafts are now open for public consultation, with the deadline for submitting comments set for February 24, 2026.