ECHA Adds Three New Chemicals to REACH Candidate List in June 2025
On 25 June 2025, the European Chemicals Agency (ECHA) added three hazardous chemicals to its Candidate List of Substances of Very High Concern (SVHCs) under the REACH regulation. This update brings the total number of entries on the list to 250. The three new substances have been included based on their toxicity. This update aims to ensure that companies manage the risks associated with these chemicals and provide information on their safe use to customers and consumers. Newly added substances: Two of these substances are classified as very persistent and very bioaccumulative, meaning they remain in the environment for a long time and accumulate in living organisms. These are commonly used in cosmetics, personal care products, and automotive care products. The third substance is classified as toxic for reproduction, posing risks to fertility and fetal development. It is typically used in textile treatment products and dyes. Under REACH, suppliers of articles containing an SVHC in concentrations above 0.1% (weight by weight) are required to provide safety data sheets and safe use instructions to customers and consumers. Substances added to the Candidate List may eventually be included in the Authorisation List, meaning companies will need to apply for authorisation from the European Commission to continue using them. ComplianceXL provides expert knowledge and consulting services on hazardous substances added to the Candidate List. We support companies in managing compliance with EU regulations and help maintain up-to-date supplier certificates and declarations as part of a robust compliance data management strategy. FAQs: 1. What industries are most affected? Industries most impacted include cosmetics and personal care, textiles and dyes, and automotive and lubricants. 2. What should companies do after a substance is added to the Candidate List They should check for the substance in their products, update safety information, notify ECHA if needed, and prepare for possible authorisation requirements.
Chromium (VI) Restriction Proposal: Advancing Health and Environmental Safety
Chromium (VI) compounds are widely used in industries such as metal plating, leather tanning, and pigment manufacturing. While they serve important industrial purposes, these substances are known to be highly toxic and carcinogenic. To mitigate the risks, the European Chemicals Agency (ECHA) has proposed stricter restrictions to limit human and environmental exposure. Chromium (VI) is a well-documented health hazard. Prolonged exposure can lead to severe respiratory issues, skin ulcerations, and cancers, especially lung cancer. Both industrial workers and consumers of chromium-treated products face significant risks. Additionally, Chromium (VI) can contaminate soil and water, resulting in long-term environmental damage. ECHA’s proposed restrictions aim to limit the production, sale, and use of Chromium (VI)-containing products within the EU chemical regulations. The proposal encourages industries to transition to safer alternatives and implement stricter workplace safety measures. Risk assessments and public consultations are integral parts of the regulatory process. Key Benefits The proposed EU Chemical restrictions on Chromium (VI) represent a proactive step toward safeguarding public health and the environment. With strong support from regulatory bodies and industry stakeholders, this move supports a shift toward a safer, more sustainable future. FAQs: 1: Why is Chromium (VI) considered so dangerous? It is a known carcinogen and poses serious health risks through inhalation, ingestion, or skin contact. 2: Will the restrictions apply to all industries? Only to those that currently use Chromium (VI). Many have already begun transitioning to safer alternatives. 3: Are safer substitutes available? Yes. Particularly in sectors like plating and coating, several viable alternatives are already in development or use.
ECHA Proposes Three New Substances for SVHC Classification
On February 28, 2025, the European Chemicals Agency (ECHA) launched a public consultation for the 33rd update of the Candidate List under REACH authorization. Norway and Sweden have proposed the inclusion of three new substances. Stakeholders can submit their comments until April 14, 2025. Substances of Very High Concern (SVHCs) are identified based on their hazardous properties. This identification process is open for public consultation, allowing stakeholders to provide feedback on dossiers submitted by EU Member States or ECHA. In this update, three substances have been proposed for SVHC classification due to their classification as very persistent and very bioaccumulative (vPvB) and their toxicity for reproduction: Impact of SVHC Listing If a substance is designated as an SVHC, it is added to the Candidate List and may later be included in the Authorisation List. Once listed for authorization, its use is prohibited unless companies apply for and obtain permission from the European Commission. Obligations for companies include: If the Member State Committee (MSC) approves the nomination of these three substances, the SVHC count will increase from 247 to 250 by mid-2025. Compliance XL provides expert consulting services for REACH compliance, including SVHC assessments, supplier declarations, and compliance data management. Our team ensures businesses remain up to date with the latest REACH regulatory requirements. FAQs: 1.What is an SVHC? A Substance of Very High Concern (SVHC) is a chemical that poses significant risks to human health or the environment, requiring regulatory attention under REACH. 2.How can I participate in the consultation? Stakeholders can submit feedback on the proposed substances during the consultation period. Detailed information, including the proposals and supporting documents, is available on the ECHA website.
ECHA Takes on New Role to Improve Safety of Packaging Materials
The European Chemicals Agency (ECHA) is taking on a new mission to enhance packaging safety due to growing environmental concerns and increasing awareness of chemical risks. Packaging plays a crucial role in protecting products, ensuring durability, and facilitating transport. However, it also presents potential chemical hazards, especially for consumables and food. To mitigate these risks, ECHA aims to strengthen regulatory controls, reduce hazardous substances, and promote safer alternatives. The Importance of Packaging Safety While packaging is essential for maintaining product integrity, it also poses risks due to chemical migration. Toxic substances from packaging materials can leach into food, beverages, and personal care products, posing serious health threats. Key concerns include: With increasing scientific evidence and public pressure, regulators are intensifying efforts to reduce these risks. ECHA’s Expanded Role in Packaging Safety ECHA has long been at the forefront of chemical regulation in the EU, overseeing REACH (Registration, Evaluation, Authorisation, and Restriction of Chemicals) and CLP (Classification, Labelling, and Packaging) regulations. Now, under its expanded mission, ECHA is adopting a more proactive approach to packaging safety: 1.Assessing Hazardous Chemicals in Packaging: 2.Supporting the EU Packaging and Packaging Waste Regulation (PPWR): 3.Strengthening Regulations and Restrictions: 4.Enhancing Supply Chain Transparency and Accountability: Impact on Businesses Industries such as food, cosmetics, pharmaceuticals, and consumer products will be significantly affected by ECHA’s expanded role. Companies must: Failure to comply could lead to supply chain disruptions, legal repercussions, and reputational damage. Implications for Consumers ECHA’s new role in packaging safety is a significant step forward for consumers, ensuring safer and healthier packaging. Over time, consumers can expect: The Future of Packaging Safety ECHA’s enhanced responsibilities align with broader EU initiatives such as the Circular Economy Action Plan and the European Green Deal, both of which prioritize waste reduction and chemical safety. Moving forward, businesses and regulators will collaborate to drive innovation in packaging materials and ensure compliance with evolving regulations. To stay ahead, companies must swiftly adapt to these changes, meeting consumer expectations and regulatory demands. By adopting safer, more sustainable packaging solutions, businesses can enhance brand trust and contribute to a healthier, more environmentally friendly future. The regulation of chemicals in packaging materials is undergoing a significant transformation with ECHA’s expanded role in ensuring packaging safety. This shift, which includes reducing hazardous substances, increasing transparency, and promoting sustainability, benefits both businesses and consumers. Companies should embrace innovation in packaging design and proactively adjust to tightening regulations. ComplianceXL supports its clients in navigating these regulatory changes under the EU Packaging Directive, helping them enhance their business operations. FAQs: 1. What is ECHA’s new role in packaging safety? The European Chemicals Agency (ECHA) is expanding its authority to evaluate and regulate hazardous substances in packaging. This includes assessing the safety of chemicals in food-contact materials, supporting the EU Packaging and Packaging Waste Regulation (PPWR), and tightening restrictions on harmful substances. 2. When will these new regulations take effect? New packaging-related regulations under REACH and the PPWR are already being implemented. Companies should begin preparing now to comply with the upcoming changes.
Biocidal Products Regulation (EU) 528/2012 – An Overview
Biocidal products, such as disinfectants, insect repellents, and wood preservatives, play a vital role in safeguarding public health and protecting materials. However, ensuring their safety, effectiveness, and environmental sustainability necessitates stringent regulation. This is where the Biocidal Products Regulation (EU) 528/2012 (BPR) comes into effect. Biocidal products are substances or mixtures designed to control harmful organisms, including bacteria, viruses, fungi, and pests. The primary objective of the BPR is to facilitate the free movement of biocidal products within the European Union while maintaining a high level of protection for human health, animal welfare, and the environment. Special attention is given to vulnerable groups such as pregnant women and children. The regulation aims to minimize the environmental impact of biocidal products by preventing pollution of water, soil, and harm to wildlife. By standardizing the approval process across all EU member states, the BPR eliminates trade barriers and ensures uniform compliance. Before a biocidal product can be marketed in the EU, it must undergo a two-step approval process: The BPR mandates clear and accurate labeling of biocidal products to provide users with essential safety information. Even after approval, these products remain under continuous monitoring. Regulatory authorities across the EU conduct inspections to ensure compliance, and if new risks emerge, products may be restricted or withdrawn from the market. ECHA plays a pivotal role in enforcing the BPR by assessing risks associated with active substances, reviewing product applications, and maintaining a public database of approved biocidal products. Additionally, the regulation evolves with advancements in science and technology, promoting the adoption of greener and more sustainable alternatives. ComplianceXL offers expert consulting services to assist companies in meeting the requirements of the Biocidal Products Regulation. Our compliance management platform helps businesses stay up to date with regulatory obligations through due diligence, supplier engagement, and comprehensive compliance documentation. FAQs: 1. Who is responsible for enforcing the BPR? The European Chemicals Agency (ECHA) oversees the implementation of the BPR by assessing risks, reviewing product applications, and maintaining a public database of approved biocidal products. 2. Can biocidal products be sold across all EU countries? Yes, biocidal products can be marketed throughout the EU via Union Authorization. Alternatively, some products may be approved for sale in a single country through National Authorization. 3. How should biocidal products be labeled? Biocidal products must include clear labeling with instructions for use, safety precautions, and detailed product information to ensure safe and effective application.
First SVHC Update of 2025: New Substances Added to the REACH Candidate List
On January 21, 2025, the European Chemicals Agency (ECHA) expanded the Candidate List of Substances of Very High Concern (SVHCs) by adding five hazardous chemicals and updating one existing entry. With this update, the Candidate List now contains 247 entries, highlighting chemicals that pose potential risks to human health and the environment. The primary goal of this update is to ensure companies effectively manage the risks associated with these substances and provide essential safety information to customers and consumers. The newly added substances to the REACH SVHC Candidate List are: These substances have been added due to their hazardous properties. Two of them are classified as very persistent and very bioaccumulative (vPvB), while another two exhibit persistent, bioaccumulative, and toxic (PBT) characteristics. The reaction mass of triphenylthiophosphate and tertiary butylated phenyl derivatives, despite not being registered under REACH, has been identified as an SVHC to prevent regrettable substitution. Additionally, the existing entry for Tris(4-nonylphenyl, branched and linear) phosphite has been updated to indicate its endocrine-disrupting properties when it contains ≥ 0.1% w/w of 4-nonylphenol (branched and linear, 4-NP). Industry Impact : The newly added SVHCs are commonly used in lubricants, adhesives, sealants, and coatings. They also play a role in manufacturing cosmetics, personal care products, pharmaceuticals, electrical and electronic equipment, optical devices, machinery, and vehicles. Effects and Compliance Requirements The inclusion of these substances in the Candidate List encourages companies to seek safer alternatives. Under REACH regulations: Compliance XL offers expert consulting and training services to assist businesses in achieving REACH compliance. Our team supports companies in collecting and managing REACH declarations, ensuring that supplier certificates remain up to date and compliant with regulatory requirements. FAQs: 1. What is the one updated entry in the REACH Candidate List? The entry for Tris(4-nonylphenyl, branched and linear) phosphite has been revised to reflect its classification as an endocrine disruptor, particularly when it contains ≥ 0.1% w/w of 4-nonylphenol (branched and linear, 4-NP). 2. Which newly added SVHC has no active registrations but is still included in the list? The reaction mass of triphenylthiophosphate and tertiary butylated phenyl derivatives has been added despite having no active REACH registrations, as a precautionary measure to prevent regrettable substitution.
Understanding the New Classification, Labelling, and Packaging (CLP) Regulation
Adapting to evolving regulations is crucial in the realm of chemical safety. The updated guidance on the new Classification, Labelling, and Packaging (CLP) Regulation provides clearer directives and enhanced details to improve chemical hazard communication across industries. This blog breaks down the key updates, their implications, and the steps businesses need to take to remain compliant. What is the CLP Regulation? The Classification, Labelling, and Packaging (CLP) Regulation aligns with the United Nations’ Globally Harmonized System (GHS) for hazard classification and communication. It aims to standardize the classification and labelling of chemicals, ensuring consistent safety information to protect human health and the environment. Why Was This Guidance Revised? Advancements in science and shifts in industry demands necessitate updates to existing regulations. The latest revisions aim to: Key Updates in the New Guidance 1.Introduction of New Hazard Classes The updated CLP introduces new hazard classes to address previously unregulated risks, including: 2.Updated Classification Criteria Existing hazard classifications have been revised to minimize errors. Companies must reassess their chemical inventories to ensure compliance with the updated criteria. 3.New Labelling Requirements Labels must now include new hazard statements and pictograms based on the updated classifications. These changes aim to enhance the clarity and visibility of safety information for users and handlers. 4.Digital Integration The revised regulation encourages the use of digital tools, such as QR codes on packaging, to provide users with instant access to Safety Data Sheets (SDS) and supplementary hazard information. 5.Transitional Timelines The updates include phased implementation schedules to allow businesses adequate time to adapt. Each change has specific compliance deadlines, such as those for classification and labelling updates. Implications for Businesses Impact on the Supply Chain Companies must inform suppliers, partners, and customers about the required changes to ensure smooth implementation across the supply chain. Steps to Maintain Compliance The updated CLP Regulation represents a significant milestone in improving chemical safety and environmental protection, but achieving compliance can be challenging for businesses navigating the complexities of reclassification, labelling updates, and supply chain adjustments. At ComplianceXL, we specialize in simplifying regulatory compliance. From assessing your chemical portfolio to updating SDS and labels, training your teams, and ensuring seamless supply chain communication, our expert services are designed to help your business adapt efficiently to the new CLP requirements. Partner with us to stay ahead of regulatory changes, demonstrate your commitment to safety, and maintain uninterrupted operations. Let ComplianceXL be your trusted ally in achieving compliance with confidence. FAQs: 1.What is the purpose of the CLP Regulation? The CLP Regulation harmonizes the classification, labelling, and packaging of chemical substances to promote their safe use, transport, and disposal while aligning with GHS for global hazard communication consistency. 2.Who must comply with the revised CLP Regulation? The regulation applies to EU/EEA manufacturers, importers, distributors, and chemical users. Companies exporting chemicals to these regions must also comply.
New Hazardous Chemical Added to ECHA’s REACH SVHC Candidate List
The European Chemicals Agency (ECHA) is a key regulatory body within the European Union, responsible for managing the registration, evaluation, authorization, and restriction of chemicals. It plays a critical role in ensuring that chemicals used in the EU are safe for human health and the environment. ECHA’s work is central to the implementation of the REACH Regulation (Registration, Evaluation, Authorisation, and Restriction of Chemicals), which aims to protect human health and the environment from the risks posed by chemicals, while enhancing innovation and competitiveness in the EU. On November 7, 2024, the European Chemicals Agency (ECHA) added triphenyl phosphate to the Candidate List of Substances of Very High Concern (SVHC), increasing the total number of SVHCs from 241 to 242. This chemical is commonly used as a flame retardant and plasticizer in a variety of products, such as polymer formulations, adhesives, and sealants. Its inclusion is primarily due to its endocrine-disrupting properties, which can interfere with hormonal functions and potentially cause adverse health effects. The addition of triphenyl phosphate to the Candidate List has several significant implications: Compliance XL provides consulting services for REACH compliance and the collection of REACH declarations. We assist companies in maintaining up-to-date supplier certificates and declarations as part of a comprehensive compliance data management strategy. FAQs: 1. Why was triphenyl phosphate added to the Candidate List? Triphenyl phosphate was added due to its endocrine-disrupting properties, which can interfere with hormonal functions and present health risks. 2. What are the obligations of companies when a substance is added to the Candidate List? Companies must provide safety data sheets and instructions for the safe use of products containing the substance. They must also notify ECHA if the substance is present in concentrations exceeding 0.1% by weight. 3. What is the outlook for triphenyl phosphate? Triphenyl phosphate may eventually be moved to the Authorisation List, which would require companies to seek authorization before continuing its use.
Six New SVHCs Proposed by ECHA : Implications for Compliance and Industry Impact
In August 2024, the European Chemicals Agency (ECHA) launched a public consultation on a proposal to add six new substances to the Substances of Very High Concern (SVHC) Candidate List under the EU REACH Regulation. If approved, the number of entries on the Candidate List would reach 247, increasing obligations for affected industries. The consultation, published on August 30, 2024, remains open for comments until October 14, 2024. Current Status of the SVHC List: As of June 27, 2024, the REACH SVHC Candidate List contains 241 entries. Inclusion of new substances places immediate regulatory responsibilities on companies that use these substances in their products above the specified thresholds. These obligations include customer notifications and required submissions to the SCIP (Substances of Concern in Products) Database. Newly Proposed SVHCs and Their Properties: ECHA’s proposal includes six substances, flagged for their potentially hazardous characteristics, including reproductive toxicity, persistence, bioaccumulation, toxicity (PBT), very persistent, very bioaccumulative (vPvB) properties, and endocrine-disrupting effects. These substances are: The Impact of New SVHC Inclusions: If a substance is officially identified as an SVHC, it is added to the Candidate List, which serves as a stepping stone to possible inclusion on the Authorisation List. When a substance is on the Authorisation List, companies must seek authorisation from the European Commission for continued use; otherwise, its use is restricted or prohibited. Immediate Obligations for Companies: For suppliers, the addition of new SVHCs triggers several requirements: Benefits of Compliance: Identifying and addressing SVHCs helps companies proactively manage potential risks associated with hazardous substances, aligning with EU’s stringent environmental and public health standards. Proactive compliance not only supports legal requirements but also bolsters customer trust and brand reputation, as consumers increasingly prioritize sustainable, safe products. Compliance XL provides comprehensive consulting services for REACH compliance, including support with REACH declarations and SVHC data management. Our services include maintaining supplier certificates and declarations to ensure up-to-date compliance records, simplifying the ongoing obligations companies face as they adapt to regulatory updates. As the regulatory landscape evolves, understanding and adhering to REACH requirements is essential. Compliance XL is committed to helping companies stay ahead of regulatory changes, ensuring smooth operations and compliance. Reach out to learn how we can assist with your REACH compliance strategy and data management needs. FAQs: 1.Who needs to comply with REACH? Companies or individuals that import, manufacture, use or place substances, mixtures or articles on the EU market must be compliant with the REACH regulation. 2.How can companies ensure compliance with REACH? Companies can ensure compliance by registering their substances with ECHA, maintaining up to date SDS, keeping detailed records, and staying informed about regulatory changes.
Upcoming PFAS Restriction Proposal: Everything You Need to Know
In response to growing concerns about the environmental persistence and potential health risks of per- and polyfluoroalkyl substances (PFAS), the European Chemicals Agency (ECHA) is taking action within the ambit of REACH, the European Union’s regulatory framework for chemicals. PFAS, known for their unique properties like resistance to heat, water, and oil, are extensively utilized across various industries. Yet, their durability and possible adverse effects on health have prompted urgent regulatory scrutiny. Problem: The contamination caused by PFAS is linked to numerous health problems, such as cancer, immune system disturbances, and developmental issues. Due to their environmental persistence, PFAS accumulate in living organisms and extensively contaminate water, soil, and wildlife. The lack of thorough regulatory measures has enabled PFAS to permeate a wide range of consumer goods, industrial activities, and materials, thereby presenting significant threats to human health and the ecological balance. Solution: Upcoming Meetings: March 2024: Discussions on PFAS hazards in consumer mixes, cosmetics, and ski wax (reported by RAC) and the general strategy (exclusive to SEAC). June 2024: Debate on risks in metal plating and metal goods production (by RAC). September 2024: Focus on petroleum and mining, food contact materials and packaging, and textiles, furniture, leather, clothes, and carpets (TULAC). The repercussions : ECHA’s proactive approach towards evaluating and potentially restricting PFAS under REACH underscores a commitment to tackling emerging chemical risks and safeguarding human health and the environment. Collaboration among regulatory authorities, scientific committees, industry stakeholders, and the public is paramount to ensuring the effectiveness and feasibility of proposed PFAS restrictions. ComplianceXL aids businesses in achieving PFAS regulatory compliance by compiling pertinent data related to PFAS for their products. Moreover, we offer ongoing maintenance services to ensure the integrity and currency of regulatory documentation for our clients moving forward. FAQs: Q: What specific sectors are being addressed in the upcoming committee meetings? A: The sectors under discussion include consumer mixtures, cosmetics, ski wax, metal plating, metal product manufacturing, textiles, upholstery, leather, apparel, carpets, food contact materials, packaging, petroleum, and mining. Q: How will feedback from the consultation process be incorporated into the proposal? A: The five national authorities responsible for the proposal will revise and update it based on the comments received during the consultation. This updated proposal will serve as the foundation for the scientific committees’ evaluations and subsequent recommendations.