All regulatory updates
1373 results found
RoHS Annex III entry 7(c)-I split into 7(c)-V and 7(c)-VI for lead exemptions
Commission Delegated Directive (EU) 2025/2363 has restructured the RoHS Annex III exemption for lead in glass and ceramic components. The original broad exemption Entry 7(c)-I has been split into two separate entries: 7(c)-V for lead in glass applications and 7(c)-VI for lead in ceramic applications. This restructuring provides more precise scope definitions for each exemption category, improving clarity for compliance determinations. Manufacturers using lead in glass or ceramic components must verify which specific sub-exemption applies to their products.
EU adopts Delegated Directive 2025/1802 for lead exemption in high melting temperature solders
Commission Delegated Directive (EU) 2025/1802, adopted on 8 September 2025 and published on 21 November 2025, renews and amends the RoHS exemption for lead in high melting temperature solders (lead-based alloys containing 85% or more lead by weight). The exemption renewal is recorded in Annex III of Directive 2011/65/EU and applies to electrical and electronic equipment placed on the EU market. Manufacturers using high-temperature lead-based solder alloys should verify their compliance status against the updated exemption terms and any new expiry dates.
Draft Commission delegated regulation text published (Ares) proposing Annex I listing and UTC limits for LC‑PFCAs (C9–C21), their salts and related compounds
A European Commission draft delegated regulation (Ares document) sets out proposed amendments to Regulation (EU) 2019/1021 to list long-chain perfluorocarboxylic acids (LC‑PFCAs; C9–C21), their salts and related compounds in Annex I (Part A), and proposes unintentional trace contaminant (UTC) limit values applicable to substances, mixtures and articles. The draft text also includes derogation/exemption concepts (e.g., isolated intermediate use under strictly controlled conditions; time-limited allowances for certain semiconductor spare-part/repair uses). Compliance teams should use this draft to anticipate likely final EU restriction scope, trace-limit testing needs, and potential supply-chain redesign and customer declarations.
European Commission opens public feedback on draft delegated amendments to list chlorpyrifos, MCCPs and LC‑PFCAs in Annex I (consultations close 19 Dec 2025)
The European Commission opened ‘Have your say’ public feedback consultations on draft delegated regulations to amend Annex I of Regulation (EU) 2019/1021 (EU POPs Regulation) to add chlorpyrifos, medium-chain chlorinated paraffins (MCCPs), and long-chain perfluorocarboxylic acids (LC‑PFCAs; C9–C21), their salts and related compounds. The feedback period is indicated as open until 19 Dec 2025. For compliance teams, this signals likely upcoming EU-wide prohibitions and associated unintentional trace contaminant (UTC) limits affecting substances, mixtures and articles; companies potentially impacted should review draft texts and submit technical feedback (e.g., trace contamination feasibility, supply-chain impacts, and any requested derogations).
Commission Delegated Directive (EU) 2025/2364 amends RoHS Annex III lead alloy exemptions
Commission Delegated Directive (EU) 2025/2364 restructures and renews RoHS Annex III exemptions 6(a), 6(b), and 6(c) for lead as an alloying element in steel, aluminium, and copper. Key changes include: exemption 6(a) for lead in steel is not renewed and expires December 11, 2026; new sub-exemptions 6(a)-I and 6(a)-II are created for specific applications expiring June 30, 2027; exemption 6(b) for lead in aluminium is partially renewed with new subcategories; exemption 6(c) for lead in copper alloys is renewed until June 30, 2027. Manufacturers must review product portfolios to identify items relying on expiring exemptions.
European Commission opens 'Have your say' consultations on draft delegated acts to add chlorpyrifos, MCCPs, and LC‑PFCAs to Annex I
The European Commission launched public consultations ('Have your say' initiatives) on draft delegated acts proposing to amend Annex I of Regulation (EU) 2019/1021 (EU POPs Regulation) to address Stockholm Convention COP-12 listings by adding chlorpyrifos, medium-chain chlorinated paraffins (MCCPs), and long-chain perfluorocarboxylic acids (LC‑PFCAs), their salts and related compounds. For compliance teams, this signals pending EU-wide prohibitions/restrictions and associated trace contaminant limit-setting for substances/mixtures/articles once adopted; companies should consider submitting comments and beginning impact assessments for materials, product portfolios, and supply chains.
European Commission draft delegated regulation proposes adding MCCPs to Annex I (Part A) with 0.1% w/w UTC limit and time-limited exemptions (consultation-stage)
A draft Commission Delegated Regulation (consultation-stage) proposes amending Regulation (EU) 2019/1021 to add medium-chain chlorinated paraffins (MCCPs) to Annex I (Part A), aligning with Stockholm Convention COP-12 Decision SC‑12/10. The draft proposes an unintentional trace contaminant (UTC) limit of 0.1% by weight (1,000 mg/kg) for MCCPs in substances, mixtures and articles, and describes time-limited exemptions (5 years, with a possible additional 5-year extension) for certain uses (e.g., metalworking fluids in professional/industrial settings, aerospace/defence applications, medical/IVD devices, and certain spare-parts/repair contexts). Compliance teams should begin supplier engagement and material verification planning for MCCP presence and evaluate whether any exempted uses apply to their products and lifecycle/spare parts obligations if/when the amendment is finalized.
European Commission draft delegated regulation proposes adding chlorpyrifos to Annex I (Part A) with UTC limit (consultation-stage)
A draft Commission Delegated Regulation (consultation-stage) proposes amending Annex I (Part A) of Regulation (EU) 2019/1021 to list chlorpyrifos as a persistent organic pollutant, aligning with Stockholm Convention COP-12 Decision SC‑12/9. The draft indicates chlorpyrifos would be listed without EU-specific exemptions (noting it is not approved under EU plant protection products/biocides regimes) and would set an unintentional trace contaminant (UTC) limit applicable to substances, mixtures, and articles for enforcement of the general prohibition. Compliance teams should anticipate future supply-chain restrictions and need to verify chlorpyrifos absence/trace levels in articles and mixtures once finalized and published.
European Commission opens consultation on draft initiative to add LC‑PFCAs (C9–C21), their salts and related compounds to Annex I (Part A) (consultation-stage)
The European Commission opened a 'Have Your Say' consultation (initiative page) related to a draft delegated amendment to the EU POPs Regulation (EU) 2019/1021 concerning long-chain perfluorocarboxylic acids (LC‑PFCAs; described in secondary sources as C9–C21 PFCAs), their salts and related compounds, with the objective of listing them in Annex I (Part A) (prohibited POPs). Compliance teams should monitor the final delegated act text once adopted/published for specific unintentional trace contaminant limits, any exemptions, and application dates affecting substances/mixtures/articles containing LC‑PFCAs and related substances.
European Commission opens public consultations on draft amendments to list chlorpyrifos, MCCPs and LC‑PFCAs (C9–C21) in Annex I
The European Commission launched three separate Better Regulation “Have Your Say” public consultations on draft delegated regulations to amend Annex I (Part A) of Regulation (EU) 2019/1021 (EU POPs Regulation) to add: (1) chlorpyrifos, (2) medium‑chain chlorinated paraffins (MCCPs), and (3) long‑chain perfluorocarboxylic acids (LC‑PFCAs, C9–C21), their salts and related compounds. If adopted, these amendments would prohibit manufacture, placing on the market and use in the EU, subject to any specified derogations/UTC limits in the final text. Compliance teams should monitor the consultation outcomes and prepare for potential EU supply‑chain restrictions and trace-contaminant limit requirements affecting substances, mixtures and articles.
Washington adopts WAC 173-337 amendments restricting PFAS in consumer products
Washington adopted amendments to Chapter 173-337 WAC (Safer Products Restrictions and Reporting) restricting the manufacture, sale, and distribution of consumer products containing intentionally added PFAS. The rule restricts PFAS in apparel and accessories made from leather, natural textiles, synthetic textiles, or technical textiles; automotive washes; and cleaning products, with product bans effective January 1, 2027. The amendment adds a 50 ppm total fluorine threshold—products testing above this level are presumptively deemed to contain intentionally added PFAS subject to reporting requirements or bans unless the manufacturer submits a statement that PFAS were not intentionally added.
CARB Notice of Public Hearing for Landfill Methane Regulation Amendments
CARB announced a public hearing on November 20, 2025 to consider proposed amendments to the Regulation on Methane Emissions from Municipal Solid Waste Landfills (LMR). The hearing provides opportunity for stakeholder input on proposed changes to the landfill methane regulatory requirements.
Washington Adopts PFAS Restrictions in 12 Product Categories Under WAC 173-337
Washington Department of Ecology adopted amendments to Chapter 173-337 WAC (Safer Products Restrictions and Reporting) on November 20, 2025, restricting intentionally added PFAS in 12 consumer product categories including apparel, cleaning products, and automotive washes. Sales prohibition takes effect January 1, 2027. The rule adds a 50 ppm total fluorine threshold for presumptive determination of intentionally added PFAS and requires manufacturer reporting for 9 additional product categories.
CNCA sets phased transition timeline for China RoHS conformity assessment to GB 26572-2025
China's Certification and Accreditation Administration (CNCA) issued Announcement No. 44 of 2025 establishing a phased transition timeline for conformity assessment under China RoHS. From publication until December 31, 2025, companies may use GB/T 26572-2011, GB/T 26572-2011 with Amendment 1, or GB 26572-2025 for conformity assessment. From January 1, 2026 to July 31, 2027, companies must use either GB/T 26572-2011 with Amendment 1 or GB 26572-2025. From August 1, 2027 onward, only GB 26572-2025 may be used. Products that completed conformity assessment under GB/T 26572-2011 before January 1, 2026 must complete reassessment by January 1, 2027. This affects all electrical and electronic product manufacturers and importers placing products on the Chinese market.
EPA Seeks Comment on 1,2-Dichloroethane Draft Risk Evaluation
EPA has announced the availability of and is soliciting public comment on the draft risk evaluation for 1,2-Dichloroethane under TSCA. This draft risk evaluation assesses whether the chemical presents unreasonable risk of injury to health or the environment under its conditions of use. Public comments will inform EPA's final risk determination.
ECHA issued recommendation (18 Nov 2025) to include four Candidate List SVHCs in REACH Annex XIV (Authorisation List)
ECHA published its recommendation dated 18 November 2025 to the European Commission to include four SVHCs in REACH Annex XIV (Authorisation List): Melamine; S-(tricyclo[5.2.1.0²,⁶]deca-3-en-8(or 9)-yl) O-(isopropyl/isobutyl/2-ethylhexyl) O-(isopropyl/isobutyl/2-ethylhexyl) phosphorodithioate; Diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide; and Barium diboron tetraoxide. This is a pre-legislative step that can lead to future authorisation requirements (latest application/sunset dates) if adopted into Annex XIV by the European Commission. Compliance teams should track these substances and evaluate potential substitution/authorisation strategies.
ECHA issues 12th recommendation for Annex XIV inclusion
ECHA has issued its 12th recommendation for priority substances to be included in REACH Annex XIV (Authorisation List). The recommendation, finalized on 18 November 2025, followed a public consultation from 7 February 2024 to 7 May 2024. Substances recommended include melamine (EC No. 203-615-4) and others from the Candidate List. The European Commission will now decide whether to add these substances to Annex XIV. If adopted, companies using these substances will need to apply for authorisation before the latest application date and cease use after the sunset date unless authorisation is granted.
ECHA publishes 12th Recommendation for Annex XIV inclusion
On 18 November 2025, ECHA published its 12th Recommendation for inclusion of substances in Annex XIV (Authorisation List) under REACH. Substances recommended include Diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide (EC 278-355-8, CAS 75980-60-8), identified as toxic for reproduction under Article 57(c). The European Commission will make the final decision on inclusion. Companies using these substances should prepare for potential authorisation requirements if the Commission adopts the recommendation.
ECHA publishes 12th Annex XIV recommendation for authorization list
ECHA published its 12th Recommendation for inclusion of substances in Annex XIV (List of Substances subject to Authorisation). This recommendation identifies priority substances from the Candidate List that will require authorization for continued use. Companies using or placing these substances on the EU market should prepare for potential authorization requirements, including sunset dates and application deadlines that will be set by the European Commission when adopting the recommendation.
ECHA issues 12th recommendation: four SVHCs recommended for inclusion in REACH Annex XIV (Authorisation List)
ECHA issued its final (12th) recommendation to the European Commission to include four Candidate List SVHCs in REACH Annex XIV (Authorisation List). While this is not yet a binding Annex XIV amendment, it is a concrete step in the SVHC-to-authorisation pipeline and signals potential future authorisation obligations (i.e., continued use/placing on the market after any future sunset dates would require authorisation unless exemptions apply). Compliance teams should monitor the Commission’s subsequent Annex XIV amendment process and begin evaluating uses and substitution plans for the recommended substances.