On January 22, 2025, the European Union officially published the Packaging and Packaging Waste Regulation (EU) 2025/40, also known as PPWR. This regulation will fully replace the existing Directive 94/62/EC on August 12, 2026, becoming the primary EU legislation for the management of packaging and packaging waste.
Starting from April 21, 2023, two substances including 1,1,1-trichloroethane (CAS number 71-55-6) and C.I. Acid Green 73 (CAS number 129-73-7), has been added to the list of known carcinogens under Proposition 65. This list requires warning labels to be placed on goods according to the mechanism established by the California Labor Code.
ECHA’s Committee for Risk Assessment (RAC) supports the proposal to restrict polycyclic aromatic hydrocarbons (PAHs) in clay targets for shooting. The proposed restriction introduces, a 0.005 % weight by weight concentration limit for the sum of 18 indicator PAHs since its implementation; and a 1 % concentration limit after a one-year transition. The restriction aims to prevent further environmental emissions of these toxic and very persistent substances that build up in humans and animals. Many PAHs are also known to cause cancer.
Bureau of Indian Standards (BIS) is receiving comments on draft standard “ready mixed paint, air drying, red oxide-zinc chrome painting-specification” until 11 May 2022. This Draft has extended the limit of lead restriction in household coatings to industrial applications. To prevent lead exposure of children and adults and consequent adverse impact on human health and safety and because of further scope for children’s exposure to the dried paint surfaces, the lead res
A great many products exported to the U.S. are required to process FDA certification and EPA certification before entering the U.S. market. Then what do you know about FDA certification and EPA certification? As a leading product safety and regulatory consulting firm, CIRS Group is now able to provide the U.S. FDA certification and EPA certification services to help clients remove the technical barriers to trade and successfully enter the US market. What is US FDA Certificat
What is CCC? Since its introduction in December 2001, China Compulsory Certification (CCC) is a compulsory scheme based on National Chinese Standards (GB-Standards) for products listed in the Catalogue of Products subject to Compulsory Certification (“Catalogue”). CCC is similar to other certifications for product quality standardisation–such as the European CE system–but there are important differences. It has been implemented on 1 May 2002 and became fully effectiv
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